Immunization with bacterial ghost-based vaccines

ABSTRACT

Methods for improving binding of a proteinaceous substance to cell-wall material of a Gram-positive bacterium are disclosed. The proteinaceous substance includes an AcmA cell-wall binding domain, homolog or functional derivative thereof. The method includes treating the cell-wall material with a solution capable of removing a cell-wall component such as a protein, lipoteichoic acid or carbohydrate from the cell-wall material and contacting the proteinaceous substance with the cell-wall material.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. patent application Ser. No. 11/299,304, filed Dec. 9, 2005, now U.S. patent Ser. No. 7,541,039, which application and this application is a divisional of U.S. patent application Ser. No. 10/321,857, filed Dec. 16, 2002, now U.S. Pat. No. 7,067,639, issued Jun. 27, 2006, which application and this application is a continuation of International Appl'n No. PCT/NL02/000383 filed on Jun. 11, 2002, designating the United States of America, published in English on Dec. 19, 2002 as PCT International Publication WO 2002/101026 A2, which applications claim priority to EP 01202239.8, filed Jun. 11, 2001, the contents of the entirety of each of which are incorporated by reference.

STATEMENT ACCORDING TO 37 C.F.R. §1.52(e)(5)-SEQUENCE LISTING SUBMITTED ON COMPACT DISC

Pursuant to 37 C.F.R. §1.52(e)(1)(iii), a compact disc containing an electronic version of the Sequence Listing has been submitted concomitant with this application, the contents of which are hereby incorporated by reference. A second compact disc is submitted and is an identical copy of the first compact disc. The discs are labeled “copy 1” and “copy 2,” respectively, and each disc contains one file entitled “SeqListCRF.txt” which is 88 KB and created on Dec. 16, 2002.

TECHNICAL FIELD

The present invention relates generally to biotechnology, and, more particularly, pertains to a method for obtaining cell-wall material of Gram-positive bacteria with an improved capacity for binding a proteinaceous substance comprising an AcmA cell-wall binding domain, as well as pharmaceutical compositions including the obtained cell-wall material.

BACKGROUND

Heterologous surface display of proteins (Stahl and Uhlen, TIBTECH May 1997, 15, 185-192) on recombinant microorganisms via the targeting and anchoring of heterologous proteins to the outer surface or the cell wall of host cells, such as yeast, fungi, mammalian cells, plant cells, and bacteria, has been possible for several years. Display of heterologous proteins at the surface of these cells has taken many forms including the expression of reactive groups such as antigenic determinants, heterologous enzymes, single-chain antibodies, polyhistidyl tags, peptides, and other compounds. Heterologous surface display has been applied as a tool for applied and fundamental research in microbiology, molecular biology, vaccinology and biotechnology. Another application of bacterial surface display has been the development of live-bacterial-vaccine delivery systems. The cell-surface display of heterologous antigenic determinants has been considered advantageous for inducing antigen-specific immune responses in live recombinant cells used for immunization. Another application has been the use of bacterial surface display in generating whole-cell bioadsorbents or biofilters for environmental purposes, microbiocatalysts, and diagnostic tools.

Generally, chimeric proteins include an anchoring or targeting portion that is specific and selective for the recombinant organism, wherein the anchoring portion is combined with the reactive group, such as the antigenic determinant, heterologous enzyme, single-chain antibody, polyhistidyl tag, peptide, or other compound. A well-known anchoring portion comprises the so-called LPXTG (SEQ ID NO:1) box, which covalently binds to a Staphylococcus bacterial surface, i.e., in the form of a fully integrated membrane protein. In this manner, at least two polypeptides of different genetic origins may be joined by a normal peptide bond to produce a chimeric protein. For example, PCT International Patent Publication No. WO 94/18330, which relates to the isolation of compounds from complex mixtures and the preparation of immobilized ligands (bioadsorbents), discloses a method for obtaining a ligand comprising anchoring a binding protein in or at the exterior of a cell wall of a recombinant cell. The binding protein is essentially a chimeric protein produced by the recombinant cell and includes an N-terminal part derived from an antibody that is capable of binding to a specific compound, wherein the N-terminal part is joined to a C-terminal anchoring part, derived from an anchoring protein purposely selected for being functional in the specific recombinant cell chosen. PCT International Patent Publication No. WO 97/08553 discloses a method for selectively targeting proteins to the cell wall of Staphylococcus sp., using anchoring proteins which include long stretches of at least 80-90 amino acid long amino acid cell-wall-targeting signals. The signals are derived from the lysostaphin gene or amidase gene of Staphylococcus and encode for proteins that selectively bind to Staphylococcus cell-wall components.

Vaccine delivery or immunization systems with attenuated bacterial vector strains that express distinct antigenic determinants against a wide variety of diseases are currently being developed. Mucosal vaccines for nasal or oral passages using these attenuated bacterial vectors have received a great deal of attention. For example, both systemic and mucosal antibody responses against an antigenic determinant of hornet venom have been detected in mice orally colonized with a genetically engineered human oral commensal Streptococcus gordonii strain that expresses the hornet venom antigenic determinant on its surface (Medaglini et al., PNAS 1995, 2; 6868-6872). A protective immune response was also elicited by oral delivery of a recombinant bacterial vaccine that included tetanus toxin fragment C constitutively expressed in Lactococcus lactis (Robinson et al., Nature Biotechnology 1997, 15; 653-657). Mucosal immunization is considered an effective means of inducing IgG and secretory IgA antibodies directed against specific pathogens of mucosal surfaces.

Immunogens expressed by bacterial vectors may be presented in a particulate form to antigen-presenting cells, such as M-cells, of the immune system and therefore should be less likely to induce tolerance when compared to soluble antigens. Additionally, the existence of a common mucosal immune system permits immunization of one specific mucosal surface in order to induce secretion of antigen-specific IgA and other specific immune responses at distant mucosal sites. A drawback to using bacterial vectors for immunization is the potential of the bacterial strain causing inflammation or disease and potentially leading to fever or bacteremia. Instead of using attenuated bacterial strains that may become pathogenic, recombinant commensal bacteria, such as Streptococcus sp. or Lactococcus sp., may be used as vaccine carriers.

A potential problem with recombinant commensal microorganisms is that they may colonize the mucosal surfaces and generate a long-term exposure to the target antigens expressed and released by the recombinant microorganisms which may cause immune tolerance.

Additionally, the use of genetically modified microorganisms that contain recombinant nucleic acid has met considerable opposition from the public as a whole, stemming from a low-level acceptance of products which contain recombinant DNA or RNA. Similar objections exist against even the use of attenuated pathogenic strains or against proteins, or parts of proteins, derived from pathogenic strains. Further, the heterologous surface display of proteins described herein entails the use of anchoring or targeting proteins specific and selective for a limited set of microorganisms, which are of recombinant or pathogenic nature which greatly restricts their potential applications.

The protein anchor of L. lactis, AcmA (cA), its homologs and functional derivatives (PCT International Patent Publication No. WO99/25836) bind in a non-covalent manner to a wide variety of Gram-positive bacteria. Binding also occurs to isolated cell-wall material. The ligand to which the protein anchor of L. lactis binds in these cell walls is currently unknown.

The use of a gram-positive, food-grade bacterium, such as Lactococcus lactis, offers significant advantages over the use of other bacteria, such as Salmonella, as a vaccine delivery vehicle. For instance, L. lactis does not replicate in or invade human tissues and reportedly possesses low intrinsic immunity (Norton et al. 1994). Further, mucosal -delivered L. lactis that expresses tetanus toxin fragment C has been shown to induce antibodies that protect mice against a lethal challenge with tetanus toxin even if the carrier bacteria was killed prior to administration (Robinson et al. 1997). The killed bacteria still contain recombinant DNA that will be spread into the environment, especially when used in wide-scale oral immunization programs. However, the uncontrollable shedding of recombinant DNA into the environment may have the risk of being taken up by other bacteria or other microorganisms.

SUMMARY OF THE INVENTION

Disclosed is a method for improving binding of a proteinaceous substance to cell-wall material of a Gram-positive bacterium. The proteinaceous substance comprises at least one repeat, but may comprise two or three repeat sequences of an AcmA cell-wall binding domain, homolog or functional derivative thereof. The method comprises treating the cell-wall material with a solution capable of removing a cell-wall component, such as a protein, lipoteichoic acid or carbohydrate, from the cell-wall material and contacting the proteinaceous substance with the treated cell-wall material. Improved binding may be obtained by treating the cell-wall material with a solution capable of removing a cell-wall component. The cell-wall material may be subsequently stored until it is contacted with a desired fusion protein. The fusion protein may comprise an AcmA cell-wall binding domain, homolog or functional derivative thereof where the cell-wall material is contacted with the fusion protein. The method of the present invention may be used to obtain cell-wall material with an improved capacity for binding a proteinaceous substance comprising the AcmA cell-wall binding domain, homolog or functional derivative thereof.

Also disclosed is a method for removing components from a bacterial cell wall comprising treating whole cells with a solution capable of removing a cell-wall component such as a protein, lipoteichoic acid or carbohydrate from the cell-wall material. The cell-wall material obtained by the present invention yields cell-wall material with at least 20%, better 30%, best 40% or even 50% of relatively empty, but intact, cell envelopes which include inert spherical microparticles. The inert spherical microparticles will be referred to herein as bacterial “ghosts.” The term “ghosts” reflects the size and shape of the bacterium from which the ghosts are obtained.

Also disclosed is a method for obtaining cell-wall material of a Gram-positive bacterium with an improved capacity for binding with a proteinaceous substance comprising an AcmA cell-wall binding domain, homolog or functional derivative thereof. The method comprises treating the cell-wall material with a solution capable of removing a cell-wall component such as a protein, lipoteichoic acid or carbohydrate from the cell-wall material, wherein the cell-wall material comprises spherical peptidoglycan microparticles referred to herein as ghosts.

Methods to extract bacterial cell-wall material with a solution have been described in EP 0 545 352 A and Brown et al. (Prep. Biochem. 6:479, 1976). A method to obtain purified soluble peptidoglycan from bacteria by exposure to TCA has been disclosed. The cited references describe procedures in which cells are mechanically disrupted, wherein the resulting cell fragments are treated with TCA to extract peptidoglycans from the cell wall. The cited methods provide a peptidoglycan preparation and a lysed, randomly fragmented cell-wall preparation from which cell-wall components have been removed. However, these methods do not yield ghosts. Furthermore, the methods do not allow targeting with a proteinaceous substance comprising an AcmA cell-wall binding domain, homolog or functional derivative thereof.

The method of the present invention is aimed at yielding ghosts from which cell-wall components have been removed. The use of ghosts for display of proteinaceous substances has advantages over the use of the disrupted cell-wall material. For example, binding the proteinaceous substance to bacterial ghosts results in a higher packing density when compared to binding a substance to mechanically disrupted cell-wall material. A high density surface display of proteins is favorable for application in industrial processes. In one embodiment, the present invention discloses a method for obtaining the cell-wall material not involving rupture.

Cell-wall material obtained by mechanical disruption methods suffers from several practical drawbacks. Because cells are completely broken with mechanical disruption, intracellular materials are released from the cell and cell-wall fragments need to be separated from a complex mixture of proteins, nucleic acids, and other cellular components. The released nucleic acids may increase the viscosity of the solution and complicate processing steps, especially chromatography. The cell debris produced by mechanical lysis also often includes small cell fragments which are difficult to remove. These problems are overcome when ghosts are produced using methods of the present invention. The uniform composition of a ghost preparation including particle size and shape offers other advantages for subsequent purification and isolation steps. The invention thus discloses a method of obtaining cell-wall material not involving rupture of the cell wall, wherein the resulting cell-wall material comprises ghosts.

The use of bacterial ghosts is often preferable when compared to the use of mechanically disrupted cell-wall bacteria for the surface display of immunogenic determinants. In contrast to mechanical disruption procedures, ghosts are produced by a process that preserves most of the bacteria's native spherical structure. Bacterial ghosts are better able to bind to and/or are more easily taken up by specific cells or tissues than mechanically disrupted cell-wall material. The ability of bacterial ghosts to target macrophages or dendritic cells enhances their functional efficacy. Thus, the non-recombinant, non-living ghost system disclosed by the present invention is well suited as a vaccine delivery vehicle. Accordingly, the invention discloses a method for obtaining ghosts, wherein the ghosts have an improved capacity for binding with a proteinaceous substance and have an enhanced induction of the cellular immune response.

The invention also discloses a method for binding a proteinaceous substance to the cell-wall material of a Gram-positive bacterium, wherein the proteinaceous substance comprises an AcmA cell-wall binding domain, homolog or functional derivative thereof. The method comprises treating the cell-wall material with a solution capable of removing a cell-wall component such as a protein, lipoteichoic acid or carbohydrate from the cell-wall material, and subsequently contacting the proteinaceous substance with the cell-wall material. The cell-wall material comprises ghosts which have been produced by the present invention which does not involve rupture of the bacterial cell-wall.

In another embodiment, the solution capable of removing the cell-wall material has a pH that is lower than the calculated Pi value of the AcmA cell-wall binding domain, homolog or functional derivative thereof. Particularly, the solution comprises an acid such as acetic acid (HAc), hydrochloric acid (HCl), sulphuric acid (H₂SO₄), trichloro acetic acid (TCA), trifluoro acetic acid (TFA), and monochloroacetic acid (MCA). The concentration of the acid in the solution will be dependent on the desired pH value which may be determined by calculation using a computer program such as DNA star or Clone Manager. For instance, when the calculated pI is >8, pH values of about 6 to 4 may suffice for effecting appropriate binding. When pI values are calculated to be lower, such as around 6, pH values of 3-4 may be selected. When domains with calculated pI values ranging from 8 to 12 are encountered, using the solution comprising 0.06 to 1.2 M TCA, or comparable acid, may suffice.

The binding may be improved by heating the cell-wall material or ghosts in the solution. However, precise requirements for the heating may vary depending on the cell-wall material or ghosts. However, heating for 5-25 minutes at approximately boiling temperature (i.e., 100° C.) will often generate the desired cell-wall material with improved binding capacity. The cell-wall material may then be washed and pelleted (e.g., by centrifugation) from the treatment solution and subsequently stored (e.g., by freezing or freeze-drying) until further use. Such cell-wall material includes spherical peptidoglycan microparticles that usually reflect the size and shape of the bacterium from which they were obtained.

In one embodiment, the cell-wall material is derived from a Lactococcus, a Lactobacillus, a Bacillus or a Mycobacterium sp. The cell walls of Gram -positive bacteria include complex networks of peptidoglycan layers, proteins, lipoteichoic acids and other modified carbohydrates. Generally, chemical treatment of the cell-wall material may be used to remove cell-wall components such as proteins, lipoteichoic acids and carbohydrates, wherein the chemical treatment yields purified peptidoglycan (Morata de Ambrosini et al. 1998). Sodium dodecyl sulphate (SDS) is also commonly used to remove proteins. Trichloro acid (TCA) is known to specifically remove lipoteichoic acids and carbohydrates from cell-wall isolates. Phenol, formamide and mixtures of chloroform and methanol are other examples of organic solvents that may be used to enhance the purification of peptidoglycan.

In the present invention, the effect of the pretreatment of whole cells of gram-positive bacteria with these and other chemicals in relation to binding technology provides the possibility to obtain bacterial ghosts or cell-wall material derived from the bacteria which possess new traits (i.e., different binding properties) without the introduction of recombinant DNA.

In another embodiment, the present invention discloses the incorporation of cell-wall material with improved binding capacity for AcmA-type anchors into a composition, such as a pharmaceutical composition, with a proteinaceous substance comprising an AcmA-type anchor. Reactive groups, such as antigenic determinants, heterologous enzymes, single-chain antibodies, polyhistidyl tags, peptides, and other compounds may be bound to the cell-wall material as disclosed herein by providing reactive groups with an AcmA-type anchor, and subsequently contacting the cell-wall material with the reactive groups to improve binding capacity. Other reactive groups include fluorescing protein, luciferase, binding protein or peptide, antibiotics, hormones, non-peptide antigenic determinants, carbohydrates, fatty acids, aromatic substances or reporter molecules.

In another embodiment, the invention discloses the use of cell-wall material in generating bioadsorbents or biofilters for environmental purposes, microbiocatalysts, and diagnostic tools. For instance, the use of immobilized biocatalysts, such as enzymes or whole microbial cells, has increased steadily during the past decade in the food, pharmaceutical and chemical industries. The immobilized biocatalysts are more stable, easier to handle, and can be used repeatedly in industrial processes in comparison to their free counterparts. Immobilization of enzymes typically requires a chemical step to link the enzyme to an insoluble support. However, chemical treatments may negatively affect the enzymes. Alternatively, enzymes may be immobilized by incorporation in gels with the disadvantage that diffusion of the substrate into the gel slows down the process.

As disclosed herein, large-scale immobilization of enzymatically active proteins may be accomplished by surface displaying proteins on gram-positive cells or cell-wall material. For instance, the immobilization of a fusion protein comprising α-amylase or β-lactamase fused to the AcmA-protein anchor domain has been demonstrated herein in L. lactis. The addition of the AcmA-anchor fusion protein resulted in the stable attachment of heterologous proteins to the surface of L. lactis and other gram-positive bacteria. Further, pre-treating L. lactis cells and other gram-positive cells with acid as described herein results in a high density surface display of heterologous proteins and is a prerequisite for application in industrial processes. Further, the carrier or gram-positive cells may be obtained in high yield and be non-recombinant. Thus, a method disclosed herein may be used to economically produce the immobilized enzyme and make the AcmA-protein anchor a useful approach for the surface display of enzymes on gram-positive cells.

Another industrial application of an immobilized enzyme is the isomerization of glucose which is catalyzed by glucose isomerase and used during the production of high-fructose corn syrup. This process may be made economically feasible by immobilizing the glucose isomerase. The productivity of glucose isomerase is improved by increasing the stability of epoxide hydrolase in organic solvents by immobilization to microbial cells or cell-wall material as described herein.

Immobilized enzymes may also be used to treat waste water or industrial effluent. For instance, industrial effluents containing low value chemicals produced during synthesis of the commodity chemicals epichlorohydrin and propylene oxide may be treated by using immobilized haloalkane dehalogenase to recycle these low value products into the manufacturing process.

The invention further discloses chimeric or hybrid AcmA-type anchors for the preparation of a composition that has new binding properties. The AcmA-type anchors can be divided into two groups of hybrids based on their pI (see, Table 3). A large group includes hybrids with a pI higher than 8, but lower than 10, and a smaller group includes hybrids with a relatively low pI (i.e., <5). Hybrid AcmA-type anchors are disclosed with at least one AcmA-type domain and a relatively high calculated pI, and another AcmA-type domain is disclosed with a relatively lower calculated pI. The resulting hybrid anchor has an intermediate calculated pI which is useful when release of the bound proteinaceous substance at a higher pH is contemplated. Such a composition may be routed through the stomach, which has a relative low pH, such that the composition releases its anchor bound reactive groups in the intestines, which have a higher pH.

The invention also discloses a proteinaceous substance comprising an AcmA cell-wall binding domain, homolog or functional derivative thereof wherein the binding domain is a hybrid of at least two different AcmA-type cell-wall binding domains, homologs or functional derivatives thereof. The proteinaceous substance may comprise an AcmA cell-wall binding domain, homolog or functional derivative thereof where the binding domain is a hybrid of at least two different AcmA repeat sequences and has a calculated pI lower than 10. For instance, a hybrid protein anchor including the A1 and A2 repeat sequences of AcmA and the D1 repeat sequence of AcmD may be constructed. Such a hybrid domain may comprise at least one AcmA-type domain with a relatively high calculated pI and another AcmA-type domain with a relatively lower calculated pI. The domain with the relatively high pI may be derived from, or be functionally equivalent to, the AcmA-type domain of the lactococcal cell-wall hydrolase AcmA. Of course; many other domains with a high pI are known, such as those disclosed in Table 3. A domain with a relatively low pI may be derived from, or be functionally equivalent to, the AcmA-type domain of the lactococcal cell-wall hydrolase AcmD. However, other domains with relatively low pI are known, including those disclosed in Table 3.

The invention further discloses a proteinaceous substance comprising a hybrid domain with at least two stretches of amino acids, wherein each stretch corresponds to a domain repeat sequence and is located adjacent to each other. The stretches may be separated by one or more amino acid residues of a short distance, i.e., 3-6 to 10-15 amino acids apart, by a medium distance, i.e., 15-100 amino acids apart, or by longer distances, i.e., >100 amino acid residues apart.

In another embodiment, the invention discloses a proteinaceous substance with a hybrid AcmA domain that further comprises a reactive group. Reactive groups that may be used include, without limitation, antigenic determinants, heterologous enzymes, single-chain antibodies or fragments thereof, polyhistidyl tags, fluorescing proteins, luciferase, binding proteins or peptides, antibiotics, hormones, non-peptide antigenic determinants, carbohydrates, fatty acids, aromatic substances, inorganic particles such as latex, and reporter molecules. The reactive group may also include AcmA cell-wall binding domains, homologs or functional derivatives thereof wherein the binding domain is a hybrid of at least two different AcmA cell-wall binding domains, homologs or functional derivatives thereof that are useful in heterologous surface display and are broadly reactive with cell-wall components of a broad range of micro-organisms. As used herein, the AcmA cell-wall binding domains, homologs and functional derivatives thereof will also be referred to as hybrid AcmA domains.

The invention further discloses reactive groups which are non-protein moieties, including substances such as antibiotics, hormones, aromatic substances, inorganic particles, or reporter molecules. The substances may be constructed by binding an antibiotic, such as penicillin, tetracycline or various other antibiotics, a hormone, such as a steroid hormone, or any other compound to a binding domain produced by the present invention. Such binding may be achieved using various techniques known in the art and may function to label or “flag” the binding domain. For instance, a binding domain may be bound to a reporter molecule such as fluorescent nanoparticles, i.e., FITC or HRPO, wherein tools are generated that may be used in diagnostic assays to detect microorganisms possessing peptidoglycan. Similarly, a binding domain may be bound to an antibiotic and used for in vivo parenteral administration into the bloodstream of humans or animals, or used in vitro to bind microorganisms with peptidoglycan in order to increase the concentration of the antibiotic around the microorganism which may be killed by the antibiotics.

The invention further discloses a reactive group which is a protein moiety which may include, without limitation, antigenic determinants, enzymes, single-chain antibodies or fragments thereof, polyhistidyl tags, fluorescing proteins, binding proteins or peptides. For instance, a protein including a reactive group which is another protein or polypeptide is disclosed. The invention also discloses a nucleic acid molecule encoding the protein produced using the methods of the invention. Such a nucleic acid molecule, comprising single-stranded or double-stranded DNA, RNA or DNA-RNA duplex, comprises nucleic acid sequences which encode a hybrid binding domain. The nucleic acid molecule may also comprise nucleic acid sequences encoding the reactive group polypeptide and may further comprise other nucleic acid sequences encoding a signal peptide comprising promoter sequences or regulatory nucleic acid sequences.

A vector comprising a nucleic acid molecule encoding a proteinaceous substance provided by the invention is also disclosed. Examples of vectors include, without limitation, a plasmid, a phage or a virus, wherein the vectors may be constructed using nucleic acids of the invention and routine skills known in the art. Viral vectors include baculovirus vectors or comparable vector viruses through which a protein produced by the present invention may be expressed or produced in cells, such as insect cells.

A host cell or expression system including a nucleic acid molecule or a vector produced using methods of the present invention is also disclosed. The host cell expressing a protein of the present invention may be a microorganism to which the protein is attached. The host cell, or expression system, may be a Gram-positive bacterium, a Gram-negative bacterium, a yeast cell, an insect cell, a plant cell, a mammalian cell, or a cell-free expression system, such as a reticulocyte lysate. The host cell or expression system may be constructed or obtained using a nucleic acid or vector of the present invention and routine skills known in the art.

In a further embodiment, the invention discloses a pharmaceutical composition comprising cell-wall material with an improved binding capacity with an immunogen bound thereto which may be useful for vaccination purposes, i.e., a vaccine. The vaccine may be used to invoke immunity against pathogens, such as malaria, which undergo life cycle stages where the pathogen is not in the blood but hides in cells.

The vaccines may be delivered to mucosal surfaces instead of being injected since mucosal surface vaccines are easier and safer to administer. An L. lactis-derived cell-wall material may be used for mucosal vaccination since this bacterium is of intestinal origin and no adverse immune reactions are generally expected from L. lactis.

The vaccine of the invention may also be administered by injection. When the vaccine is administered through injection, cell-wall material may be derived from a Mycobacterium sp. since mycobacterial cell-wall preparations have beneficial adjuvant properties. The mycobacterial cell-wall vaccine may be mixed with the proteinaceous substance carrying the immunogenic determinants used in the vaccine.

A vaccine produced using a method of the present invention will likely have a reduced risk of generating undesirable immune responses against cell-wall compounds of unwanted immunogens because the unwanted immunogens are not included in the vaccine.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. Schematic map of plasmid pNG3041 that encodes the reporter protein MSA2::cA that is secreted as a proprotein using the lactococcal PrtP signal- and prosequences (PrtP.sspro). Pnis represents the nisin inducible promoter of the nisA gene. T represents the transcriptional terminator. CmR is the chloramphenicol resistance gene. repC and repA are genes involved in the replication of the plasmid.

FIG. 2A. Fluorescence microscopic images of bacterial cells with externally bound MSA2::cA. Lb. curvatis, Lb. sake and L. lactis cells that were not pretreated prior to binding.

FIG. 2B. Fluorescence microscopic images of bacterial cells with externally bound MSA2::cA. L. lactis cells that were TCA-pretreated prior to binding. The light colored areas indicate the position where the reporter protein MSA2::cA binds. The difference between L. lactis cells that were not pretreated with TCA (in FIG. 2A) and those that were TCA pretreated is apparent (in FIG. 2B).

FIG. 3. Western blots of chemically pretreated L. lactis cells that were washed after the pretreatment and incubated with MSA2::cA to allow binding. Unbound MSA2::cA was removed by washing. The drawing shows the MSA2::cA that was bound to the chemically pretreated cells and detected using an antibody specific for MSA2. The different pretreatments are indicated above the lanes. MSA2::cA is produced by the producer cells as a proprotein, pro-MSA2::cA. Some pro-MSA2::cA is present in the medium used for binding and binds as indicated by the arrow. A membrane bound protease, HtrA, of the producer cells cleaves off the prosequence, resulting in mature MSA2::cA, which also binds to the pretreated cells as indicated by the asterisk. HtrA also cleaves off the repeats of the cA anchor. Since there are three repeats, MSA2 proteins of several sizes are present in the medium of the producer. As long as more than one repeat is present, binding can still occur. The double asterisks point to MSA2::cA from which one or two repeats have been cleaved. M is a molecular weight marker. The molecular weights are indicated in the left margin. The two blots have different signal intensities. As a reference, both blots contain the same TCA-pretreated samples. The difference in signal intensity is due to differences in stain developing time. It is apparent that the TCA and other acid pretreatments produce pronounced effects on the subsequent binding of MSA2::cA. The conclusions for all chemical pretreatments are summarized in Table 1.

FIG. 4. Coomassie stained SDS-PAGE gel with chemically pretreated L. lactis cells. Pretreatments: (1) no-treatment; (2) HCl; (3) H₂SO₄; (4) HAc; (5) TFA; and (6) TCA. It is apparent that treatment of the cells with HCl, H₂SO₄, TFA or TCA significantly removes an amount of protein from the cells.

FIG. 5. Western blot of L. lactis cells pretreated with different TCA concentrations and externally bound with MSA2::cA. Arrow and asterisks: as in FIG. 3. Pretreatments: (1) no TCA treatment; (2) 1% TCA; (3) 5% TCA; (4) 10% TCA; and (5) 20% TCA. An increase in the binding of MSA2::cA is shown to correlate with increasing amounts of TCA used in the pretreatment.

FIG. 6. Alignment of cA repeats with cD repeats. AcmA (A1) (SEQ ID NO:16) is aligned to AcmD (D1) (SEQ ID NO:19). AcmA (A2) (SEQ ID NO:17) is aligned to AcmD (D2) (SEQ ID NO:20). AcmA (A3) (SEQ ID NO:18) is aligned to AcmD (D3) (SEQ ID NO:21). Consensus repeats SEQ ID NOS: 163, 164 and 165 are aligned. The amino acids that are in agreement with the consensus sequence are shown at the bottom of the figure (defined in PCT Publication WO99/25836) are underlined. The asterisks indicate residues that are identical between the compared repeats.

FIG. 7. Binding of various anchor-fusion proteins to L. Lactis with and without TCA pretreatment. Multiple bands shown in one lane are caused by the different processed forms of MSA2 fusions. Lanes: (1) non-pretreated L. lactis+MSA2::cA; (2) non-treated L. lactis+MSA2::cD; (3) non-pretreated L. lactis+MSA2; (4) TCA-pretreated L. lactis+MSA2::cA; (5) TCA-pretreated L. lactis+MSA2::cD; and (6) TCA -pretreated L. lactis+MSA2. The effect of TCA pretreatment on the binding of MSA2::cA is shown (i.e., compare lanes 1 and 4). A minor improvement for MSA2::cD and no improvement for MSA2 without anchor is observed. Since there is a signal for MSA2 without the anchor means that MSA2 by itself has a weak affinity for bacterial cell walls. However, MSA2::cD or MSA2 binding to the pretreated cells cannot be detected using fluorescence or electron microscopy (see text). The difference in results is probably due to a difference in sensitivity of the techniques.

FIG. 8. Fluorescence microscopy image of TCA-pretreated L. lactis cells incubated with MSA2::cA or MSA2::cD. Light colored areas indicate the position were the reporter fusion protein binds. It appears that binding only occurred with MSA2::cA and not with MSA2::cD.

FIG. 9A. Electron microscopy images of L. lactis cells incubated with different MSA2 constructs. The black dots represent the position of bound MSA2 fusion protein. Image A depicts non-pretreated cells incubated with MSA2::cA.

FIG. 9B. Electron microscopy images of L. lactis cells incubated with different MSA2 constructs. The black dots represent the position of bound MSA2 fusion protein. Image B depicts TCA-pre-treated cells incubated with MSA2::cA. Significant binding, shown by black dots, is only visible in the TCA-pre-treated cells incubated with MSA2::cA.

FIG. 9C. Electron microscopy images of L. lactis cells incubated with different MSA2 constructs. The black dots represent the position of bound MSA2 fusion protein. Image C depicts TCA-pre-treated cells incubated with MSA2::cD.

FIG. 9D. Electron microscopy images of L. lactis cells incubated with different MSA2 constructs. The black dots represent the position of bound MSA2 fusion protein. Image D depicts TCA-pre-treated cells incubated with MSA2.

FIG. 10. Binding of different anchor-fusion proteins to B. subtilis with and without TCA pretreatment. The drawing is a Western blot similar to FIGS. 3 and 7. Lanes: (1) non-pretreated cells+MSA2::cA; (2) non-pretreated cells+MSA2::cD; (3) non-pretreated cells+MSA2; (4) TCA-pretreated cells+MSA2::cA; (5) TCA-pretreated cells+MSA2::cD; (6) TCA-pretreated cells+MSA2; and (7) non-pretreated B. subtilis (negative control). TCA pretreatment improves the binding of MSA2::cA in a manner similar to L. lactis (i.e., compare lanes 1 and 4). Only background binding is observed for MSA2::cD and MSA2 without anchor.

FIG. 11. Fluorescence microscopy image of MSA2::cA binding to Lb. casei with or without TCA pretreatment. The light colored areas represent bound MSA2::cA. TCA pretreatment improves binding of MSA2::cA and Lb. casei.

FIG. 12. Fluorescence microscopy image of MSA2::cA and MSA2::cD binding to M. smegmatis pretreated with TCA. The light colored areas represent bound MSA2 fusion protein. As illustrated, only MSA2::cA binds.

FIG. 13. Western blot of L. lactis cells with externally bound MSA2::cA treated with LiCl or stored under different conditions. The bands in the various lanes represent the amount of MSA2::cA that remained bound to the TCA-pretreated cells. Arrow and asterisks: as in FIG. 3. Lanes: (1) marker; (2) non-pretreated L. lactis incubated without MSA2::cA; (3) non-pretreated L. lactis incubated with MSA2::cA; (4) TCA-pretreated L. lactis incubated with MSA2::cA; (5) TCA-pretreated L. lactis incubated with MSA2::cA, subsequently washed with 8 M LiCl; (6) TCA-pretreated L. lactis incubated with MSA2::cA, subsequently stored in water for 3 weeks at 4° C.; (7) TCA-pretreated L. lactis incubated with MSA2::cA, subsequently stored in 10% glycerol for 3 weeks at −80° C.; and (8) TCA -pretreated L. lactis incubated with MSA2::cA, subsequently stored in water for three weeks at −80° C. As illustrated, TCA pretreatment improves binding of MSA2::cA to L. lactis cells (i.e., compare lanes 3 and 4). Washing with 8 M LiCl and storage in water for 3 weeks at 4° C. has minor effects on the bound MSA2::cA (i.e., compare lane 4 with 5 and 6). Storage at −80° C. has no effect on the bound MSA2::cA (i.e., compare lane 4 with 7 and 8).

FIG. 14A. Fluorescence microscopy image of MSA2::cA surface expression in the recombinant strain NZ9000(pNG3041). The light colored areas indicate the position of MSA2 fusion protein. The recombinant strain producing MSA2::cA has the protein on the surface in some specific spots.

FIG. 14B. Fluorescence microscopy image of MSA2::cP surface expression in the recombinant strain NZ9000(pNG3043). The recombinant strain producing MSA2::cP has more on the surface organized in several areas.

FIG. 14C. Fluorescence microscopy image of MSA2::cA binding to TCA pretreated L. lactis cells. The surface of the TCA-pretreated non-recombinant L. lactis with bound MSA2::cA is completely covered with the protein.

FIG. 15. Western blots of L. lactis total protein extracts reacted with rabbit immune serum diluted at 1:100. 0: preimmune serum. 2 and 3: serum after the second and third immunization, respectively. A1: subcutaneously immunized rabbit with NZ9000Δ acmA (pNG3041) cells (recombinant, MSA2::cA surface anchored). B1: subcutaneously immunized rabbit with NZ9000ΔacmA (negative control). C2: orally immunized rabbit with NZ9000ΔacmA(pNG3043) cells (recombinant, MSA2::cP surface anchored). E1: orally immunized rabbit with TCA-pretreated NZ9000ΔacmA to which MSA2::cA had been externally bound (non-recombinant, MSA2::cA surface anchored). The staining bands in the lanes illustrates that L. lactis proteins react with the indicated rabbit antiserum. It is visible that the non-recombinant TCA-pretreated strain with bound MSA2::cA (E1) evokes a minimal response to L. lactis proteins indicating that the response to the carrier is reduced, while the response to the malaria antigen is not negatively influenced (see, Table 2).

FIG. 16. Schematic representation of the domains in AcmA and AcmD. SS represents signal sequence. Both enzymes include a cell-wall binding domain that includes 3 repeats indicated by A1, 2, 3 and D1, 2, 3. The alignments of these repeats are shown in FIG. 6. In addition, an example of one of the hybrid protein anchors is described in Table 5.

FIG. 17. Western blot showing the effect of pH supernatant on binding of MSA2::cD to TCA-pretreated L. lactis cells. As previously described, the Western blot shows the amount of MSA2::cD bound by the cells. In addition, the amount of MSA2::cD that was not bound and remained in the medium after binding is shown. The arrow indicates the expected position for pro-MSA2::cD and the asterisk indicates the position of mature MSA2::cD. Lanes: (1) pH during binding 6.2, cells; (2) pH during binding 6.2, supernatant after binding; (3) pH during binding 3.2, cells; (4) pH during binding 3.2, supernatant after binding; and (5) positive control: L. lactis, TCA-pretreated with bound MSA2::cA at pH 6.2. It is visible that MSA2::cD binds better at pH 3.2 than at pH 6.2 (i.e., compare lanes 1 and 3).

FIG. 18. Western blot of medium supernatant (S) after binding to ghost cells at the indicated pH and ghost (G) with the bound protein anchor. Lanes 1 and 2 illustrate binding at pH 3; lanes 3 and 4 illustrate binding at pH 5; lanes 5 and 6 illustrate binding at pH 7. The drawing shows considerable binding at pH 5. At pH 5, the native cD anchor (D1D2D3) shows little binding. The addition of the A3 repeat, which has a high pI value, results in increased binding at pH 5.

FIG. 19. Immunization schedule. Mice immunizations were started at day 1 and repeated after 14 and 28 days. A lethal nasal challenge with S. pneumoniae was given 14 days after the last oral immunization. S.c. represents subcutaneous immunization.

FIG. 20. Serum antibody response. Mean anti-PpmA serum antibody titers. OV represents orally immunized; IN represents intranasally immunized; SC represents subcutaneously immunized; Freund's PpmA refers to soluble PpmA subcutaneously administered with Freund's complete adjuvants. High titers were obtained with the intranasally and subcutaneously administered Ghosts-PpmA::cA.

FIG. 21. Survival times. The orally vaccinated mice were challenged with a lethal dose of S. pneumonia. Mice vaccinated with soluble PpmA or Ghost alone died within 72 hours. Forty percent of the mice immunized with Ghosts-PpmA::cA survived the challenge, indicating they were protected by the vaccination.

DETAILED DESCRIPTION EXAMPLE 1 Acid Pretreatment of Gram-positive Bacteria Enhances Binding of AcmA Protein Anchor Fusions

Materials and Methods

Bacterial Strains and Growth Conditions. Lactococcus lactis strain MG1363 (Gasson 1983) or derivatives thereof, such as MG1363ΔacmA (Buist et al. 1995) or NZ9000Δ acmA, were used as recipients for binding of reporter fusion protein. NZ9000 (Kuipers et al. 1997), which carries one of the reporter plasmids, was used as a production strain. L. lactis strains were grown in M17 broth (Oxoid) supplemented with 0.5% glucose in standing cultures at 30° C. Chloramphenicol was added to the M17 medium to an end-concentration of 5 μg/ml when appropriate. For expression, mid-log phase cultures were induced for 2 hours with the culture supernatant of the nisin producing L. lactis strain NZ9700 as described by Kuipers et al. (1997). Lactobacillus casei, ATCC393, was grown in MRS broth (Oxoid) in standing cultures at 30° C. Mycobacterium smegmatis, ATCC700084, was grown in Middlebrook medium (Oxoid) at 37° C. in aerated cultures. Bacillus subtilis, 168, was grown in TY broth (per liter: 10 g tryptone, 5 g yeast extract, 5 g NaCl pH 7.4) at 37° C. in aerated cultures.

Construction of Reporter Plasmids. The merozoite surface antigen 2 (MSA2) of Plasmodium falciparum strain 3D7 (Ramasamy et al. 1999) fused to the three repeats of AcmA (MSA2::cA) was used as the reporter anchor protein. The reporter anchor protein is encoded by plasmid pNG3041 based on the nisin inducible expression vector pNZ8048 (Kuipers et al. 1997) and contains a modified multiple cloning site in which the hybrid reporter gene was cloned. An in-frame fusion of the reporter was made at the 5′ end, the lactococcal PrtP signal—and prosequence, and at the 3′ end, the AcmA protein anchor sequence. The sequence of the MSA2 gene that was included in the construct corresponds to nucleotides (nt) 61 to 708 in GenBank accession number A06129. Primers used for the amplification of the MSA2 gene were MSA2.1 (5′-ACCATGGCAAAAAATGAAAGTAAATATAGC (SEQ ID NO:2)) and MSA2.4 (5′-CGGTCTCTAGCTTATAAGCTTAGAATTCGGGATGTTGCTGCTCC ACAG (SEQ ID NO:3)). The primers contain tags with restriction endonuclease recognition sites that were used for cloning. For cloning of the PrtP signal and prosequence (nt 1206 to 1766 in Kok et al. 1988), the primers PrtP.sspro.fw (5′-CCGTCTCCCATGCAAAGGAAAAAAGA AAGGGC (SEQ ID NO:4)) and PrtP.sspro.rev (AAAAAAAGCTTGAATTCCCAT GGCAGTCGGATAATAAACTTTCGCC (SEQ ID NO:5)) were used. The primers include restriction sites that were used for cloning. The AcmA protein anchor gene fragment (nt 833 to 1875) was obtained by subcloning a PvuII-HindIII fragment from plasmid pAL01 (Buist et al. 1995). Restriction endonuclease enzymes and Expand High Fidelity PCR polymerase were used in accordance with the instructions of the supplier (Roche). The final expression vector was designated pNG3041 (FIG. 1).

A construct including a stop codon introduced after the MSA2 sequence in pNG3041 was designated pNG304. The protein secreted using this construct is substantially the same as the protein expressed from the pNG3041 plasmid except that the protein produced from pNG304 does not contain the AcmA protein anchor. The protein produced from pNG304 is used as a negative control in the binding assays. A vector was also made in which the AcmA protein anchor was exchanged for a protein anchor. The putative cell-wall binding domain of L. lactis AcmD (Bolotin et al. 2001) was cloned (nt 1796 to 2371 in GenBank accession number AE006288) using primers pACMB2 (5′-CGCAAGCTTCTGCAGAGCTCTTAGATTCTAATTGTTTGTCCTGG (SEQ ID NO:6)) and pACMB3 (5′-CGGAATTCAAGGAGGAGAAATATCAGGAGG (SEQ ID NO:7)) to produce the plasmid pNG3042. pNG3042 contains an in-frame fusion between MSA2 and the protein anchor of AcmD (MSA2::cD) and differs from plasmid pNG3041 only in the gene fragment encoding the protein anchor.

Cell Pretreatment and Binding Conditions. Chemical pretreatment of L. lactis NZ9000ÄacmA was done with 10% TCA (0.6 M) in the following manner. Cells of 0.5 ml stationary phase cultures were sedimented by centrifugation and washed once with 2 volumes of demineralized water. Cells were resuspended in 1 volume of a 10% TCA solution and incubated by placing the reaction tube in boiling water for 15 minutes. Subsequently, cells were washed once with 2 volumes PBS (58 mM Na₂HPO₄.2H₂O, 17 mM NaH₂PO₄.H₂O, 68 mM NaCl; pH 7.2) and three times with 2 volumes demineralized water. The cells were used directly for binding experiments or stored (as described herein) until further use.

The following chemicals and conditions were used to examine the effect of different chemicals on the binding capacity of L. lactis cells for AcmA-type protein anchor fusions: acetic acid (HAc), hydrochloric acid (HCl), sulfuric acid (H₂SO₄), TCA, trifluoroacetic acid (TFA), and monochloro acetic acid (MCA). The acids were used at a final concentration of 0.6 M and incubated for 15 minutes in boiling water. SDS, dimethyl formamide (DMF) and dimethyl sulfoxide (DMSO) were used at a concentration of 10%. The SDS pretreatment was incubated for 15 minutes in boiling water and DMF and DMSO treatments were incubated at room temperature for 15 minutes. Cells were also pretreated with phenol (Tris buffer saturated) and incubated for 15 minutes at 55° C. Other chemicals pretreated at the 55° C. incubation temperature were: 4 M guanidine hydrochloride (GnHCl), 37% formaldehyde, chloroform:methanol (CHCL₃:CH₃OH (2:1)) and 0.1% sodium hypochlorite (NaOCl). In addition, incubation with 25 mM dithiothrietol (DTT) for 30 minutes at 37° C. and a pretreatment with hexane (100%) were analyzed.

The effect of enzymatic pretreatment of cells with lysozyme was also tested. For lysozyme pretreatment, the cells were resuspended in buffer (20% sucrose, 10 mM Tris pH 8.1, 10 mM EDTA, 50 mM NaCl) with lysozyme (2 mg/ml) and incubated at 55° C. for 15 minutes. After the chemical and enzymatic pretreatments, the washing steps were the same as the washing steps used for the TCA-treated cells. TCA pretreatment of Bacillus subtilis, Lactobacillus casei and Mycobacterium smegmatis was done as described herein for L. lactis.

Cell-free culture supernatants containing MSA2::cA, MSA2::cD or MSA2 without anchor were incubated in four-fold excess for 10 minutes at room temperature with pretreated cells (e.g., cells from 0.5 ml culture were incubated with 2.0 ml culture supernatant). After binding, cells were sedimented by centrifugation, washed twice in 2 volumes of demineralized water, resuspended in SDS-denaturation buffer, heated for 5 minutes at 98° C., subjected to SDS-PAGE, and analyzed by Western blot analysis.

Storage Conditions. Cell-free supernatants containing MSA2::cA, MSA2::cD or MSA2 were stored at −20° C. with or without 10% glycerol prior to binding. TCA-pretreated L. lactis cells were stored at −80° C. in 10% glycerol prior to binding. TCA pretreated L. lactis cells with bound MSA2::cA were stored at +4° C. or −80° C. with or without 10% glycerol. Cells stored in 10% glycerol were washed once with 1 volume of demineralized water prior to binding.

Cell pellets (in demineralized water) of TCA-pretreated L. lactis cells with or without bound MSA2::cA were frozen by contacting the vials with liquid nitrogen and removing the water with lyophilization. Alternatively, non-frozen cell pellets were dried under vacuum at 30° C. for 2 hours prior to binding.

Western Blotting. For detection of MSA2 proteins, cell pellets corresponding to 500 μl culture were resuspended in 50 μl SDS-denaturation buffer. Cell-free culture supernatants (1 ml) were concentrated by phenol-ether precipitation (Sauvé et al. 1995), vacuum dried and resuspended in 50 μl SDS-denaturation buffer. Proteins were separated with standard SDS-PAGE techniques. After separation, proteins were electroblotted onto PVDF membranes (Roche). In immunoblots, MSA2 proteins were detected with 1:10,000 diluted rabbit MSA2-specific antiserum (Ramasamy et al. 1999) and 1:5,000 diluted anti-rabbit IgG-conjugated alkaline phosphatase (Roche) using known procedures.

Fluorescence Microscopy. 100 μl cell suspensions incubated with MSA2::cA, MSA2::cD or MSA2 fusion proteins were washed twice with demineralized water and resuspended in an equal volume of PBS containing 1% BSA and MSA2-specific rabbit antiserum diluted to 1:200. After incubation for 20 minutes at room temperature, the cells were washed three times with 2 volumes PBS. Subsequently, the cells were incubated for 20 minutes in 1 volume PBS with 1% BSA and 1:100 diluted Oregon green labeled goat anti-rabbit immunoglobulin G (Molecular Probes). After washing once with 2 volumes PBS and twice with 2 volumes demineralized water, the cells were resuspended in 100 μl demineralized water. A 10 μl aliquot of the resuspended cells was spread onto a Polysin microslide (Menzel-Gläser), air dried, and examined under a fluorescence microscope (Zeiss).

Electron microscopy. TCA-pretreated L. lactis cells incubated with MSA2::cA, MSA2::cD or MSA2 were collected and washed as described herein. Immunogold labeling was performed on whole mount preparations of glutaraldehyde fixed cells on Formvar-carbon coated nickel grids using Auroprobe 15 nm goat anti-rabbit IgG gold marker (Amersham). Primary antibodies against MSA2 were diluted 1:1000 in PBS-glycine buffer. The labeled samples were stained with 0.1% uranyl acetate (W/V in water) and examined in a Philips CM10 transmission electron microscope at 100 kV.

Pretreatment of L. Lactis Cells with Different Chemicals. The cA protein anchor of L. lactis AcmA can be used to bind fusion proteins to a wide variety of Gram -positive bacteria. However, the amount of fusion protein that binds varies greatly among this group of bacteria. Binding of MSA2::cA that covers the entire cell surface of some lactobacilli was observed, whereas other bacteria such as L. lactis showed only limited localized binding (FIG. 2A). This phenomenon may be due to the fact that the cell walls of some bacterial species contain components that interfere with cA anchor binding. Since chemicals like SDS, TCA, chloroform/methanol and others may be used to remove components from isolated bacterial cell walls (Morata de Ambrosini et al. 1998), the effect of the removal of cell-wall components from L. lactis whole cells on the binding of the reporter fusion protein MSA2::cA was investigated. L. lactis cells were pretreated as described herein with various chemicals or with lysozyme.

FIG. 3 shows typical Western blots of pretreated whole cells to which MSA2::cA was bound. Mature MSA2::cA migrates at a position of a 75 kDa protein (indicated by an asterisk). The arrow represents MSA2::cA that contains the PrtP prosequence. The double asterisks represent MSA2::cA from which one or two of the repeats have been removed. A cell membrane anchored protease HtrA has been shown to be involved in processing proproteins and in removing repeats from AcmA (Poquet et al. 2000). From the results of FIG. 3, it may be concluded that pretreatment with TCA (lanes 8 and 16 contain the same samples, the difference in signal intensity is due to differences in stain developing time), HCl, H₂SO₄ and HAc substantially improves the subsequent binding of MSA2::cA (compare with the negative control in lane 15). Other tested acids, TFA and MCA, had similar effects (not shown). Phenol, GnHCl, formamide and chloroform/methanol pretreatments showed a moderate improvement of binding (lanes 4, 5, 6, 7, respectively). Minor binding improvements were observed after pretreatment with SDS, DMF, DMSO and DTT. The results are summarized in Table 1. Based on the results, it appears that pretreatment of L. lactis cells with the acids TCA, TFA, MCA, HCl, H₂SO₄ and HAc are the most effective agents for improving binding of cA anchor fusion proteins to lactococcal cells. Acids such as TCA are known to remove lipoteichoic acids from cell walls.

Whether proteins are removed from the cell walls by these acid treatments was also analyzed. FIG. 4 shows a Coomassie stained gel of lysed pretreated cells. Most of the acid treatments, except for HAc, removed a substantial amount of proteins from the lactococcal cells. Since HAc removed only a trace amount of proteins (compare lane 1 and 4) and SDS pretreatment (which is known to remove proteins from the cell walls) showed only a minor improvement of MSA2::cA binding (FIG. 3, lane 1), it may be concluded that removal of proteins from the cell wall is not critical for improving the binding of cA anchor fusions. This conclusion may be due to the fact that lipoteichoic acids or carbohydrates occupy sites in the cell walls of L. lactis that interfere with efficient binding. Alternatively, acid pretreatment may result in altering the compactness of peptidoglycan strands that make cA binding sites more available.

TCA pretreatment was also used in all other experiments. The optimal TCA concentration in the boiling procedure was determined. TCA percentages of 1, 5, 10 and 20% were tested. Although 1% TCA pretreatment already showed a significant improvement in binding of MSA2::cA and 5% TCA pretreatment showed a further increase, no further improvement was observed at concentrations higher than 10% TCA (FIG. 5). Therefore, the boiling procedure with 10% TCA was selected as the standard procedure for the experiments.

The binding characteristics of the lactococcal cA homolog cD in an MSA2 fusion were analyzed using the standard TCA pretreatment procedure. Two of the three AcmD repeats are highly homologous to those of AcmA. An alignment is shown in FIG. 6. Secreted MSA2 without an anchoring domain was included in these experiments as a negative control. In Western blots, the effect of TCA pretreatment on the binding of MSA2::cA was evident (FIG. 7, compare lanes 1 and 4). The effect of TCA pretreatment was also studied using fluorescence microscopy (FIG. 2, compare L. lactis in A and B; FIG. 8) and electron microscopy (FIG. 9, compare A and B). Independent of the technique used, the effect of TCA pretreatment on the binding of MSA2::cA can be detected.

The binding of MSA2::cD to non-TCA-pretreated L. lactis cells was low as detected in Western blots (FIG. 7, lane 2) and was undetectable in fluorescence microscopy and electron microscopy (FIG. 9A). TCA pretreatment only had minor effects on the intensity of the MSA2::cD signal in Western blots (FIG. 7, lane 5). At the same time, no MSA2::cD specific signal associated with the pretreated cells could be observed in fluorescence microscopy (FIG. 8) and only low levels of labeling were observed in electron microscopy (FIG. 9C). Some cell-associated signal was observed for MSA2 without anchoring domain for both non-TCA pretreated and TCA-pretreated L. lactis cells (FIG. 7, lanes 3 and 6, respectively). However, for MSA2::cD, this was not observed in fluorescence microscopy (not shown) and only minor labeling signals were found in electron microscopy (FIG. 9D). Taken together, it may be concluded that: (i) the reporter protein MSA2 does have some low degree of affinity for bacterial cell walls that can be detected in Western blots; (ii) the cA anchor domain specifically stimulates the binding of the reporter fusion to non-pretreated cells; (iii) chemical pretreatment, especially with acids, enhances this binding; and (iv) the cD anchor domain does not promote binding of fusion proteins under the conditions applied.

The fluorescence microscopic images and electron microscopic images of TCA pretreated lactococcal cells (FIGS. 2, 8 and 9) showed that pretreatment leaves the integrity of the cell intact. However, cells are no longer viable (plating efficiency 0) and therefore may be considered as inert spherical peptidoglycan microparticles with a diameter of approximately 1 μm, “ghost cells.”

Binding to Other Gram-Positives. The binding of MSA2::cA, MSA2::cD and MSA2 without anchor domain to the Gram-positive bacteria B. subtilis, Lb. casei and M. smegmatis was also analyzed. FIG. 10 shows a Western blot summarizing binding of MSA2::cA, MSA2::cD and MSA2 to non-pretreated and TCA-pretreated B. subtilis cells. As for L. lactis, an increase in binding is observed for MSA2::cA. An MSA::cA specific signal could also be visualized in fluorescence microscopy of non-pretreated B. subtilis cells, but with a highly improved signal for the TCA-pretreated cells (not shown). Binding of MSA2::cD and MSA2 to non-pretreated or TCA-pretreated cells could not be demonstrated in fluorescence microscopy (not shown).

Similar results were obtained for Lb. casei and M. smegmatis. The improved binding of MSA2::cA to TCA-pretreated Lb. casei cells is shown in FIG. 11. For MSA2::cD and MSA2, no fluorescence signals were detected (not shown). The TCA pretreatment of M. smegmatis also had a positive effect on the binding of MSA2::cA, whereas no binding was observed for MSA2::cD or MSA2 (FIG. 12). Taken together, it may be concluded that acid pretreatment, such as with TCA, improves the binding of cA protein anchor fusions to the cell surface of Gram-positive bacteria.

Binding strength and storage conditions. The strength of the MSA2::cA binding to TCA-pretreated L. lactis cells was analyzed with a treatment of LiCl after the binding. LiCl is commonly used to remove proteins from bacterial cell walls. From the Western blot of FIG. 13, it may be concluded that 8 M LiCl partially removes MSA2::cA from the L. lactis cells (compare lanes 4 and 5). Therefore, although MSA2::cA binds non-covalently to cell walls, the binding interactions are most likely very strong.

Cell-free culture supernatants with MSA2::cA were stored with or without 10% glycerol at −20° C. MSA2::cA stored in this manner for several weeks had the same capacity to bind to TCA-pretreated L. lactis cells (not shown).

TCA-pretreated L. lactis cells with bound MSA2::cA were stored for 3 weeks at +4° C. in demineralized water or at −80° C. in demineralized water with or without 10% glycerol. The samples were analyzed in Western blots. Storing pretreated cells with bound MSA2::cA for 3 weeks in water at +4° C. only resulted in a loss of signal of about 50% (FIG. 13, compare lanes 4 and 6). Whether this loss of signal was due to degradation or due to release of the protein into the water was not determined. Storage at −80° C. with or without 10% glycerol had no effect on the binding (FIG. 13, compare lanes 4, 7 and 8).

In addition, the effects of drying and lyophilization on the binding of MSA2::cA to TCA-pretreated L. lactis cells were studied. Drying of pretreated cells had no observable negative effect on binding of MSA2::cA afterwards. Dried pretreated cells with bound MSA2::cA could be resuspended in water without losing bound fusion protein. This was also observed for lyophilized cells with bound MSA2::cA. Lyophilization of TCA-pretreated cells prior to binding resulted in loss of the binding capacity for MSA2::cA (results not shown).

From these data, it may be concluded that: (i) in spite of the non-covalent character of cA anchor binding to cell walls, the binding is very strong; (ii) cell-free culture supernatants can be stored safely at −20° C.; and (iii) drying of TCA-pretreated cells provides an efficient and simple method for storage of such cells either with or without bound cA-anchor fusions.

EXAMPLE 2 Oral Immunizations of Rabbits with Non-recombinant Lactococcus Lactis Preloaded with the Plasmodium falciparum Malaria Antigen MSA2 Fused to the Lactococcal AcmA Protein Anchor

In Example 1, a technology is described that efficiently binds protein hybrids when externally added to the cell surface of non-recombinant gram-positive bacteria by means of an AcmA-type protein anchor. This technology provides the possibility to provide bacteria or bacterial cell walls with new traits without introducing recombinant DNA into them. The immunogenicity in rabbits of the Plasmodium falciparum merozoite surface protein, MSA2 of strain 3D7 (Ramasamy et al. 1999), presented on the cell surface of non -recombinant non-living L. lactis cells as an AcmA anchor fusion protein was investigated.

Materials and Methods

Bacterial Strains and Growth Conditions. The L. lactis strain which produces MSA2::cA, the strain's growth conditions, the induction for expression, the TCA pretreatment of the L. lactis recipient cells and the binding of MSA2::cA to the cells was described in Example 1 with the following modification: a ratio of 1 (TCA-pretreated cells) to 5 (cell-free culture supernatant with MSA2::cA) was used for binding. An L. lactis NZ9000 strain carrying plasmid pNG3043 was used as a positive control in the immunization experiments (was positive in a previous, unpublished experiment). Plasmid pNG3043 encodes an MSA2 hybrid protein that contains the lactococcal PrtP cell-wall anchoring domain at its C-terminus (MSA2::cP) instead of the AcmA protein anchor. The PrtP cell-wall anchoring domain contains the LPXTG (SEQ ID NO: 1) motif that enables a membrane-linked sortase to covalently couple the protein to the cell wall (Navarre and Schneewind 1994). The cP domain used in construct pNG3043 corresponds to nt 6539 to 6914 in Kok et al. (1988). Primers used for the amplification of this fragment were PrtP.cwa.fw3 (5′-ATATAAAGCTTGCAAAGTCTGAAAACGAAGG (SEQ ID NO:8)) and PrtP.cwa.rev (5′-CCGTCTCAAGCTCACTATTCTTCACGTTGTTTCCG (SEQ ID NO:9)). The primers include restriction endonuclease recognition sites for cloning. Plasmid pNG3043 differs from plasmid pNG3041 in the cell-wall binding domain. Growth conditions and induction of expression of strain NZ9000ΔacmA(pNG3043) were the same as for strain NZ9000Δ acmA(pNG3041).

Rabbit Immunizations. Ten barrier-reared, New Zealand white rabbits obtained from Harlan laboratories, The Netherlands, were used in groups of 2 for experimental immunizations. The care and use of animals were according to WHO guidelines (WHO/LAB/88.1). The rabbits were ear bled prior to immunization to obtain preimmune sera. Details of the rabbits and immunogens are as follows:

Rabbits A1 and A2 were subcutaneously immunized with NZ9000Δ acmA(pNG3041) cells (recombinant, MSA2::cA partly surface anchored).

Rabbits B1 and B2 were subcutaneously immunized with NZ9000ΔacmA (negative control).

Rabbits C1 and C2 were orally immunized with NZ9000ΔacmA(pNG3043) cells (recombinant, MSA2::cP surface anchored).

Rabbits D1 and D2 were orally immunized with NZ9000ΔacmA(pNG3041) cells (recombinant, MSA2::cA surface anchored).

Rabbits E1 and E2 were orally immunized with TCA treated NZ9000ΔacmA to which MSA2::cA had been bound from NZ9000ΔacmA(pNG3041) culture supernatant (non-recombinant, MSA2::cA surface anchored).

Stocks of NZ9000ΔacmA(pNG3043) with MSA2::cP expressed at its surface were stored in aliquots of 10¹¹ cells in growth medium containing 10% glycerol at −80° C. The cells remain viable under these conditions and retain MSA2 on the surface as demonstrated by immunofluorescence (not shown). The first immunization was carried out with freshly grown bacteria. For subsequent immunizations, stocks of bacteria were freshly thawed, washed and resuspended in buffer at the appropriate concentration for immunizations.

On the other hand, the non-pretreated NZ9000ΔacmA (negative control), the non-pretreated NZ9000ΔacmA(pNG3041) and the TCA-pretreated NZ9000ΔacmA with the externally bound MSA2::cA were prepared daily from fresh cultures.

Subcutaneous injections were performed with a total of 5×10⁹ cells in 100 μl PBS without any adjuvant into two sides on either side of the spine. The subcutaneous injections were repeated two more times at three-week intervals. Prior to oral immunization, the rabbits were deprived of water and food for two to four hours. The rabbits were then fed 5×10¹⁰ cells resuspended in 1 ml of 0.5% sucrose. Each dose was repeated for three successive days to obtain reproducible oral immunization. Altogether, three series of oral immunizations were given at three-week intervals. Adverse effects consequent to the immunizations, including granulomas at the sites of subcutaneous injections, were not observed, indicating that L. lactis was well tolerated by the animals.

Serum Antibody Responses. Rabbits were ear bled two weeks after each immunization to obtain sera for antibody assays. The sera were stored at −20° C. until use. Ten-fold serial dilutions of the antisera in 2% BSA in PBS were used in immunofluorescence assays (IFA) to determine the titer of the antibodies against MSA2 on the surface of 3D7 P. falciparum merozoites. IFA was performed on acetone-methanol fixed late stage 3D7 P. falciparum parasites as previously described (Ramasamy 1987). For detection of antibody isotypes, Oregon Green conjugated goat anti-rabbit Ig (Molecular Probes) was used as the second antibody. For detection of IgG antibodies, a fluorescein conjugated, affinity purified, mouse monoclonal with specificity against rabbit IgG chains (Rockland) was used.

Results and Discussion

Surface Expression of MSA2 in Different L. Lactis Strains. Coomassie staining of SDS-PAGE gels and fluorescence microscopy were used to determine, in a semi-quantitative way, the number of MSA2 molecules expressed and surface exposed by the recombinant lactococcal strains carrying plasmid pNG3041 or pNG3043 that produce MSA2::cA or MSA2::cP, respectively, and by the non-recombinant TCA-pretreated L. lactis cells to which MSA2::cA had been bound from the outside. The recombinant strains were estimated to produce approximately 1.4×10⁵ molecules of MSA2::cA or MSA2::cP. The surface exposure of MSA2::cA and MSA2::cP differed considerably as shown by fluorescence microscopy in FIG. 14. The non-recombinant TCA-pretreated L. lactis cells with bound MSA2::cA showed a uniform staining of the entire cell surface. However, the semiquantitative SDS-PAGE analysis indicated that about 1×10⁴ molecules of MSA2::cA per cell were represented.

Accordingly, it may be concluded that the number of surface-exposed MSA2::cA and MSA2::cP on the recombinant lactococcal strains is less than 10% of the total number of molecules produced by these strains. The other molecules are most likely trapped in the membrane or the cell wall. Similar observations were made by Norton et al. (1996) for the expression of TTFC fused to the cP cell-wall anchoring domain. In that study, only membrane-associated or cell-wall-associated TTFC could be demonstrated and no surface-exposed TTFC::cP was demonstrated. Thus, it appears that binding from the outside to TCA-pretreated cells is a more efficient method to surface-exposed proteins on L. lactis cells.

Anti-MSA2 Antibody Responses in Orally Immunized Rabbits. Characteristics of the anti-MSA2 antibody response to the immunizations are summarized in Table 2. The oral immunizations with the recombinant L. lactis that produces MSA2::cP (rabbits C1 and C2) were done before (unpublished results) and used as a positive control. In the previous experiment, a similar antibody response was found. The present experiment showed that specific antibodies against near native MSA2 were detectable after two immunizations for group A, D and E rabbits, and that antibody titers increased in all instances after a third immunization. IgG antibodies were predominant after three immunizations in either the subcutaneous or oral route. A comparatively weak anti-MSA2 surface IFA, attributable to the generation of cross-reactive antibodies (as described herein), was also observed after three control subcutaneous immunizations with L. lactis cells alone.

Taken together, the results indicate that: (i) MSA2 produced by lactococcal cells elicits serum antibodies that recognize native P. falciparum parasite MSA2; (ii) MSA2-specific T_(h) cells are activated through mucosal immunization due to the presence of systemic IgG antibodies (Table 2) that can be boosted (unpublished results); and (iii) oral immunizations with MSA2::cA bound to non-recombinant non-living TCA-pretreated L. lactis cells are as efficient in evoking specific serum antibody responses as the live recombinant strain producing MSA2::cA that was administered subcutaneously or orally, or as efficient as the live recombinant strain producing MSA2::cP that binds MSA2 covalently to its cell wall delivered orally.

Anti-lactococcal Antibody Responses. Western blots (FIG. 15) demonstrated significant antibody responses against L. lactis antigens after two and three immunizations of the rabbits. The responses were notably greater after subcutaneous (group A and B rabbits) than oral immunization with L. lactis (group C rabbits). Oral immunization with the TCA-pretreated lactococcal cells (group E rabbits) elicited antibodies that reacted at a lower intensity with fewer L. lactis antigens than oral immunization with viable L. lactis cells. This is most likely due to the fact that proteins are removed from the lactococcal cells by the TCA pretreatment (see, Example 1). The lower anti-carrier response observed for the TCA-pretreated (non -recombinant) cells renders this type of delivery vehicle more suitable for repeated immunization strategies than its untreated (recombinant) counterpart.

EXAMPLE 3 pH-dependent Cell-wall Binding of AcmA Protein Anchor Homologs and Hybrids

The cell-wall binding domain or anchor of the lactococcal cell-wall hydrolase unization strategies than AcmA includes three repeats of 45 amino acids that show a high degree of homology (Buist et al. 1995). These three repeats belong to a family of domains that meet the consensus criteria as defined in PCT publication WO 99/25836 and can be found in various surface-located proteins in a wide variety of organisms. Another feature that most of these domains have in common is that their calculated pI values are high, approximately 8 or higher (Table 3). The pH used in previous binding experiments with MSA2::cA (i.e., Examples 1 and 2) was approximately 6, indicating that the binding domain was positively charged.

The AcmA protein anchor homolog of the lactococcal cell-wall hydrolase AcmD (cD) (Bolotin et al. 2001) also includes three repeats (FIG. 16) with a calculated pI that is lower (approximately pI 3.8) than that of the cA domain (Table 4). Consequently, the cD anchor was negatively charged at the binding conditions used in Example 1. No binding of the MSA2::cD reporter protein occurred under these conditions as demonstrated herein. Therefore, the influence of the pH during binding of a cD fusion protein (MSA2::cD) was investigated. Furthermore, a hybrid protein anchor including the three cD repeats and one cA repeat that has a calculated pI value that is higher than that of the cD repeats alone was constructed. The hybrid protein anchor showed better binding pH values above the pI of the cD repeats alone, indicating that the pH binding range of AcmA-type protein anchors can be manipulated by using the pI values of the individual repeats in hybrids.

Materials and Methods

Bacterial strains, growth and induction conditions, TCA pretreatment of L. lactis cells, incubation of the MSA2 protein anchor fusion proteins to TCA-pretreated cells, washing conditions, protein gel electrophoresis, Western blotting and immunodetection were the same as described herein with reference to Example 1. The cell-free culture supernatants with MSA2::cA, MSA2::cD or A3D1D2D3 have a pH of approximately 6.2. The influence of pH was examined by adjusting the pH of the cultures by the addition of HCl or NaOH to obtain the required pH.

Plasmid Constructions. The plasmid that expresses the MSA2::cD fusion was described herein with reference to Example 1. Plasmid pPA43 is based on the same expression plasmid and contains an in-frame fusion of the lactococcal signal sequence of Usp45 (ssUsp; van Asseldonk et al. 1990. Gene 95: 155-160), the c-myc epitope for detection purposes, the A3 cA repeat and repeats D1, D2 and D3 of cD. Primers used for cloning A3 were cA repeat3.fw (CCG TCT CCA ATT CAA TCT GCT GCT GCT TCA AAT CC (SEQ ID NO: 10)) and cA repeat3.rev (TAA TAA GCT TAA AGG TCT CCA ATT CCT TTT ATT CGT AGA TAC TGA CCA ATT AAA ATA G (SEQ ID NO: 11)) (the primers include the A3 specific sequences). The primers used for cloning the three cD repeats were cDrepeat1.fw (CCGTCTCCAATTTCAGGAGGAACTGCTGTTACAACTAG) (SEQ ID NO: 12) and cDrepeat3.rev (TAATAAGCTTAAAGGTCTCCAATTCCAGCAACTTGCAAAACTTCTCCTAC) (SEQ ID NO: 13) (the primers include the cD specific sequences).

Results and Discussion

Binding of MSA2::cD at Low pH. Since binding of MSA2::cD was not observed at a pH (the pH of the culture medium after growth and induction is about 6.2) higher than the calculated pI for the cD domain (i.e., pI 3.85), binding was studied when the pH of the medium was adjusted to pH 3.2. TCA-pretreated L. lactis cells were used as the binding substrate and the relative amounts of bound MSA2::cD were analyzed in Western blots. The amounts of unbound reporter protein remaining in the culture supernatant after binding were also analyzed. FIG. 17 shows a clear increase in bound MSA2::cD when binding is performed at pH 3.2 (compare lanes 1 and 3). At the same time, less unbound reporter protein remained in the supernatant (compare lanes 2 and 4). This result indicates that positive charges are important for binding of cA-type anchoring domains.

Binding of cAcD Hybrid Anchors. Analysis of the pI values of the cA homologs in Table 3 indicates that two classes of repeats can be distinguished: a majority (99 out of 148) of homologs that have a high pI value (>8) and a smaller group (33 out 148), of which cD is a representative, that has pI values lower than 6. Based on the experimental results, it is shown that these types of anchoring domains only bind to bacterial cell walls at a pH that is lower than the anchoring domains pI. Notably, most cell-wall binding domain homologs include repeats with a pI that are representatives of one of the two groups, i.e., only repeats with a high or low pI. Some proteins with cell-wall binding domains, e.g., those of DniR of Trepanoma pallidum and an amidase of Borrelia burgdorferi, include repeats with high and low pI. Since the binding pH of such “natural hybrid” cell-wall binding domains is below the intermediate pI value of the total number of repeats present in the domain, a hybrid cell-wall protein anchor was constructed using the cA and cD repeats with an intermediate pI value. Table 5 lists the native AcmA and AcmD anchors and a number of examples of cA/cD hybrids. The constructed hybrid protein anchor (A3 D1D2D3) has a calculated pI value of approximately 5.1. A protein anchor including only D1D2D3 shows little binding at a pH above its calculated pI (as described herein). The A3 (pI 10) domain shows similar binding at pH 5 and pH 7.

The binding of the hybrid anchor A3D1D2D3 was tested at pH 3, pH 5 and pH 7. At pH 3, most protein had been bound to the ghost cells (FIG. 18). At pH 5, there was considerable binding (+/−40%), whereas there was only minimal binding at pH 7 (+/−20%). This result indicates the pH range of binding for cD repeats was shifted to higher pH values by the addition of one cA repeat (A3) that caused a shift in calculated pI values of 3.8 to 5.1. The increase of binding at pH 5 for the A3D1D2D3 hybrid cannot be attributed to binding of the A3 repeat alone. If this was the case, then the same level of binding should occur at pH 7 since the A repeats show the same binding at these pH values. In addition, the increased binding at pH 5 is not an additive effect in the sense that an extra binding domain results in increased binding. It has previously been shown that addition of one repeat to the cA anchor did not result in increased binding. The binding at the higher pH values of the A3D1D2D3 repeats, as compared to the D1D2D3 repeats alone, thus may be attributed to the increase in the calculated pI value of the hybrid cA/cD anchor. This demonstrates that pH binding properties of these types of protein anchors may be manipulated on the basis of the pI values of individual repeats present in the hybrid anchor.

EXAMPLE 4 Induction of Cellular Immune Responses in Mice after Oral Immunizations with Lactococcal Ghosts Displaying the Malaria Plasmodium Falciparum Antigen MSA2 Fused to the Lactococcal AcmA Protein Anchor

Non-genetically modified non-living Lactococcus lactis cells (ghosts) preloaded with the Plasmodium falciparum MSA2 antigen fused to the AcmA protein anchor (MSA2::cA) were used to orally immunize mice in a similar way as described herein with reference to Example 2. In this experiment, the question of whether immunizations through the oral route with the non-recombinant non-living Ghosts carrying MSA2::cA on their surface (Ghosts-MSA2::cA) can elicit typical Th1-type immune responses, such as IgG2 antibodies and gamma-interferon (γIFN)-producing T cells in the spleen is addressed. These responses are particularly relevant to obtain immunity for pathogens, such as malaria, that undergo stages in their life cycle where they are not in the blood but hide in cells.

Materials and Methods

Groups of five mice of different strains were used for immunization. The strains of mice used were Balb/c (with the major histocompatibility locus allotype of H2d), C57 Black (H2b), C3H (H2k) and ICR (outbred, i.e., of varying H2 types). Oral immunizations were performed at three weekly intervals. Immunizations were performed with MSA2::cA absorbed onto the surfaces of TCA-treated Lactococcus lactis cells (Ghosts-MSA2::cA) or with recombinant L. lactis that displayed MSA2 on the surface through the use of a covalently linked cell-wall anchor (L. lactis(MSA2::cP)) as described herein with reference to Example 2. The mice were tail bled to obtain serum samples two weeks after the second, third and fourth immunizations. Fecal pellets were collected and extracted to examine intestinal IgA antibody production. The mice were sacrificed at the end of each experiment and the spleens were removed for examining T-cell responses by ELISPOT. MSA2-his tag produced in E. coli was used as antigen in the ELISA and ELISPOT assay. The growth of bacterial strains and the preparation of Ghost cells were as described herein with reference to Example 2.

Results and Discussion

Kinetics and Isotypes of the Serum IgG Antibodies Generated Oral Immunizations. Differences in the kinetics of the antibody response and the isotype distribution were observed between different murine strains. The antibody response was also different when living recombinant L. lactis (MSA2::cP) or Ghosts-MSA2::cA were used as immunogens. With Ghosts-MSA2::cA, high serum antibody levels were detectable in the C3H mice after two immunizations. IgG antibodies were detectable in all four murine strains after three and four immunizations. Antibody titers were highest in C3H mice. IgG antibodies that reacted with native MSA2 on parasites were detected in the sera of immune mice by fluorescence microscopy (IFA) confirming that the immunizing form of the protein elicits biologically relevant antibodies. Control immunizations were performed with Ghosts alone where no MSA2-specific antibodies were elicited. In parallel experiments using MSA2cP as the immunogen, high serum IgG antibody levels were only seen with Balb/c mice after two immunizations. After three and four immunizations, good antibody responses developed in C3H mice. Antibody titers were highest in Balb/c mice.

Significant differences existed between the strains in the isotypes of the elicited serum IgG antibodies in response to immunization with Ghosts-MSA2::cA. Balb/c mice showed higher levels of IgG2a and IgG2b antibodies, some IgG3 antibodies and negligible IgG1, which demonstrates a possible Th1 bias. On the other hand, C57 Black and C3H mice had high IgG1, IgG2a and IgG2b, and lower IgG3 antibodies to MSA2, which is more characteristic of a mixed Th1 and Th2 response. ICR mice, as expected, showed a range of responses. Some ICR mice had the Balb/c and others the C3H/C57 Black pattern of IgG isotypes.

Formation of Mucosal Antibodies. IgA antibodies were detected by ELISA in the fecal pellets of the ICR and Balb/c mice, but were not detected in C3H or C57 Black mice when immunization was performed with living recombinant L. lactis(MSA2::cP) or Ghost-MSA2::cA.

T-Cell Responses. The increase of the intensity of the IgG ELISA reactions seen in mice immunized with Ghosts-MSA2::cA with each immunization demonstrates that boosting takes place and that a Th-dependent antibody response exists in these animals. The IgG isotype distribution further confirms this conclusion. Therefore, Th cells are generated in ICR, Balb/c, C57 Black and C3H mice.

The ELISPOT assay for detecting gamma-interferon (γIFN) producing cells detects mainly CD8⁺ Tc cells, which are an important component of the immune response to many pathogens, including malaria parasites. His-tagged MSA2 produced in E. coli was used as antigen in the assay. MSA2-specific γIFN producing cells could be detected in the spleens of Balb/c, C57 Black and C3H mice that were immunized with Ghosts-MSA2::cA. MSA2-specific γIFN producing cells were not observed in the spleens of control mice immunized with Ghosts alone or with the living recombinant L. lactis(MSA2-cP). The latter group showed a high level of non-specific γIFN producing cells. The high background observed may be due to ongoing inflammation.

The sensitization of MSA2-specific Tc cells in the spleen after immunization with the non-recombinant non-living L. lactis Ghost system carrying a foreign protein is a novel finding which is applicable to malaria since protection against sporozoite-infection is associated with γIFN producing cells being produced in the spleen.

The non-recombinant non-living Ghost system can be used in oral immunizations to elicit typical Th1-type immune responses. These types of responses are particularly relevant to obtain immunity for pathogens that undergo stages in their life cycle where the pathogens are not in the blood but rather hide in cells. The responses are more pronounced and more specific for the Ghost system than for the living recombinant system. The Ghost system has the additional advantage of eliminating the risk of spreading recombinant DNA into the environment.

EXAMPLE 5 Protection of Mice for Lethal Streptococcus pneumoniae Challenge after Oral Immunizations with Lactococcal Ghosts Preloaded with PpmA Antigen Fused to the Lactococcal AcmA Protein Anchor

Streptococcus pneumoniae is the leading etiological agent of severe infections including septicemia, meningitis, pneumonia, and otitis media. Recent studies on the molecular epidemiology and pathogenesis of S. pneumoniae have identified pneumococcal proteins with vaccine potential. One of these proteins, the protease maturation protein PpmA, has been shown to elicit immune protective potential in a mouse pneumonia model.

The non-genetically modified lactococcal ghosts have been shown to be an efficient carrier for use in oral immunizations of rabbits and mice in order to elicit strong anti-malaria immune responses. The construction of lactococcal ghosts that display the S. pneumoniae PpmA fused to the lactococcal AcmA cell-wall binding domain on their surface is described herein. The ability of these ghosts to protect orally immunized mice from a lethal nasal dose of S. pneumoniae was investigated.

Materials and Methods

Bacterial Strains and Growth Conditions. L. lactis was grown and ghost cells were prepared as described herein with reference to Example 1. S. pneumoniae was grown as described before (Gingles et al. 2001, Infect. Immun. 69: 426-434).

Construction of ppmA Protein Anchor Fusion Expression Plasmid. The expression plasmid for ppmA protein anchor fusion (PpmA::cA) was substantially similar to the expression plasmid for the MSA2 protein anchor fusion as described herein with reference to Example 2. For the secretion of PpmA::cA, the secretion signal sequence of the Usp45 protein (ssUsp) of L. lactis (van Asseldonk et al. 1990. Gene 95: 155-160) was used. The PpmA gene was cloned by PCR using primers ppmA.1 (CGGTCTCACATGTCGAAAGGGTCAGAAGGTGCAGACC) (SEQ ID NO: 14) and ppmA.2 (CGGTCTCGAATTGCTTCGTTTGATGTACTACTG CTTGAG) (SEQ ID NO:15) resulting in plasmid pPA32 which contains ppmA as an in-frame fusion with ssUsp45 and the protein anchor (ssUsp::ppmA::cA). Expression of the fusion gene results in the secreted product PpmA::cA. The primers include an Eco31I restriction enzyme recognition site that was used for digestion of the PCR fragment. This restriction digest produced NcoI and EcoRI sticky ends which were used for cloning. The primers also included the ppmA sequences. Chromosomal DNA of S. pneumoniae strain D39 was used as a template for the PCR reactions.

Preparation of the Vaccine. Three liters of M17 medium with PpmA::cA, obtained after growth and used to induce producer cells for expression of L. lactis (pPA32) was centrifuged and filter sterilized (0.2 μm) to remove the producer cells. Ghost cells were prepared from 0.5 liter of L. lactis NZ9000(ΔacmA). After binding, the ghost cells with PpmA::cA (Ghosts-PpmA::cA) were isolated by centrifugation and washed with PBS. The ghost cells were stored in PBS in aliquots of 2.5×10¹⁰ Ghosts/ml at −80° C. Two control groups included: (i) Ghosts without bound PpmA::cA; for the sample preparation, the same amounts of ghost cells were used and the same centrifugation and washing steps were performed, but the binding step was omitted; and (ii) soluble PpmA was isolated as a his-tagged fusion.

Mice Immunizations. Groups of 10 mice (CD-1) were used in the immunizations. Oral doses included 5×10⁹ Ghosts with or without PpmA::cA (50 μg) or 50 μg soluble PpmA in PBS. Nasal doses included 5×10⁸ Ghosts with or without PpmA::cA (5 μg) or 5 μg soluble PpmA. 10⁸ Ghosts-PpmA::cA (1 μg) were subcutaneously injected. For intranasal immunizations, the mice were slightly anesthetized with Isofluorane.

Intranasal Challenge. The groups of orally immunized mice were intranasally challenged 14 days after the last booster immunization with a dose of 10⁶ colony forming units (CFU) S. pneumoniae D39 as described (Kadioglu et al. 2000, Infect. Immun. 68: 492-501). Mice were monitored after the challenge for visible clinical symptoms for 7 days, at which point the experiment was ended. Mice that were alive after 7 days were considered to have survived the pneumococcal challenge and mice that became moribund during the 7-day period were judged to have reached the endpoint of the assay. The time the animal became moribund was recorded, and the animal was sacrificed by cervical dislocation.

ELISA Analysis. Serum samples were taken from each mouse before the intranasal challenge and stored at −20° C. before use. Microtiter plates were coated with 100 μg PpmA/ml in 0.05 carbonate buffer. Serial 10-fold dilutions of pooled serum of each group were incubated on the plates as described (Gingles et al. 2001, Infect. Immun. 69: 426-434). Anti-mouse immunoglobulin-horseradish peroxidase conjugate was used for detection and the absorbance was measured at 492 nm.

Results and Discussion

Serum Antibody Response. Mice were immunized orally, nasally and subcutaneously according to the scheme shown in FIG. 19. Anti-PpmA antibody titers in the blood serum were determined for each group by ELISA assays. The results are given in FIG. 20. As expected, ghosts alone administered orally or nasally, OV Ghosts or IN Ghosts, respectively, did not induce anti-PpmA antibodies. Soluble PpmA given by the nasal route resulted in only a low anti-PpmA antibody titer, which agrees with the general findings that soluble antigens are not very immunogenic when given by the mucosal routes. Ghosts-PpmA::cA provided by the oral route (OV PpmA+Ghost) induced only a low level of anti-PpmA serum antibodies. This contrasts the results for the oral immunization experiments described herein with reference to Examples 2 and 4 with MSA2::cA. However, the contrast may be antigen-type related.

Intranasal administration of Ghosts-PpmA::cA resulted in a high titer of anti-PpmA antibodies (IN PpmA+Ghosts). A high titer was also obtained by subcutaneous administration of Ghosts-PpmA::cA. These titers were lower by a factor of 5 to 10 when compared to soluble PpmA that was subcutaneously administered and formulated with the strong Freund's complete adjuvant (Peter Adrian, Erasmus University Rotterdam, The Netherlands, unpublished results). In addition, the Freund's PpmA vaccine contained 50 μg PpmA per dose, whereas the intranasally administered Ghosts-PpmA:cA contains only 5 μg/dose and the subcutaneous Ghost-PpmA::cA vaccine contains only 1 μg PpmA/dose. This result demonstrates the adjuvant effect of the ghost cells. Side effects of the orally, nasally or subcutaneously administered ghosts were not observed, which is in contrast to the severe side effects that are usually seen with the use of Freund's adjuvants.

The results demonstrate that high titer serum antibodies can be obtained by the mucosal route of administration. These data also show that ghost cells may be safely used in traditionally injected vaccines without side effects in order to induce high titer serum antibodies.

Protection Against Challenge. The mice orally immunized with soluble PpmA, Ghosts alone or Ghosts-PpmA::cA were challenged 14 days post-immunization with a lethal intranasal dose of S. pneumoniae. The mice immunized with soluble PpmA or Ghosts alone died within 72 hours after challenge. The group immunized with Ghosts-PpmA::cA showed a survival rate of 40% (FIG. 21). These results show that mucosal immunization of mice with Ghosts-PpmA induces protective immunity against a lethal S. pneumoniae challenge. In conclusion, the non-recombinant non-living Ghost system may be used to elicit high titer serum antibodies and the mucosal route of administration may be used to obtain protective immunity against a mucosally acquired pathogen.

TABLE 1 Effect of different pretreatments of L. lactis on binding of MSA2::cA. Treatment Signal on Western blot H₂O − 10% TCA (0.6 M) ++++ 0.6 M HAc ++++ 0.6 M HCl ++++ 0.6 M H₂SO₄ ++++ 0.6 M TFA ++++ 0.6 M MCA ++++ Phenol ++ 4 M GnHCl ++ 37% formaldehyde ++ CHCl₃/MeOH ++ 10% SDS + 10% DMF + 10% DMSO + 25 mM DTT + 0.1% NaHC1O* − Hexane − Lysozyme* − *Lysis of cells occurred during treatment or washing steps.

TABLE 2 MSA2 antibody titers of rabbit serum determined by IFA on Plasmodium falciparum 3D7 asexual blood stage parasites. Immunization Rabbit 3^(rd) serum Immunogen P 2^(nd) 3^(rd) IgG A1 s.c. L. lactis [MSA2::cA] 0 2 4 4 A2 s.c. L. lactis [MSA2::cA] 0 2 5 5 B1 s.c. L. lactis 0 0 1 n.d. B2 s.c. L. lactis 0 0 1 n.d. C1 oral L. lactis [MSA2::cP] 0 3 5 5 C2 oral L. lactis [MSA2::cP] 0 2 5 5 D1 oral L. lactis [MSA2::cA] 0 2 4 5 D2 oral L. lactis [MSA2::cA] 0 2 4 5 E1 oral TCA L. lactis + MSA2::cA 0 2 5 5 E2 oral TCA L. lactis + MSA2::cA 0 2 5 4 L. lactis strain used: NZ9000ΔacmA (lactococcal cells lacking the cell wall hydrolase AcmA). L. lactis [MSA2::cA] and L. lactis [MSA2::cP] are the recombinant strains with surface-expressed MSA2, cell wall anchored through the non-covalent AcmA binding domain (cA) or the covalent PrtP anchoring domain (cP), respectively. TCA L. lactis + MSA2::cA are the non-recombinant TCA-pretreated lactococcal cells to which MSA2::cA had been bound externally. P: pre-immune serum. S.C.: subcutaneous injection. Titers are expressed as the negative logarithms of the lowest ten-fold dilution of sera giving a detectable reaction on the merozoite surface. The last column represents the IgG fraction of the antibody response. 0: indicates no detectable reaction at a 1:10 dilution of the serum. n.d.: not done.

TABLE 3 AcmA cell wall binding domain homologs and their calculated pI values. (the pI values are indicated directly behind the amino acid sequences) Lactococcus * acmA YTVKSGDTLWGISQRYGISVAQIQSAN SEQ ID NO: 16 9.75 lactis NLKST IIYIGQKLVLT VKVKSGDTLWALSVKYKTSIAQLKSWN SEQ ID NO: 17 9.64 HLSSD TIYIGQNLIVS HKVVKGDTLWGLSQKSGSPIASIKAWN SEQ ID NO: 18 10.06 HLSSD TILIGQYLRIK * acmD YKVQEGDSLSAIAAQYGTTVDALVSAN SEQ ID NO: 19 4.15 SLENANDIHVGEVLQVA YTVKSGDSLYSIAEQYGMTVSSLMSAN SEQ ID NO: 20 3.78 GIYDVNSMLQVGQVLQVTV YTIQNGDSIYSIATANGMTADQLAALN SEQ ID NO: 21 4.15 GFGIND MIHPGQTIRI ØTuc2009 * lys YVVKQGDTLSGIASNWGTNWQELARQN SEQ ID NO: 22 6.31 SLSNPNMIYAGQVISFT YTVQSGDNLSSIAILLGTTVQSLVSMN SEQ ID NO: 23 3.45 GISNPNLIYAGQTLNY Ø-LC3 * lysB YIVKQGDTLSGIASNLGTNWQELARQN SEQ ID NO: 24 6.31 SLSNPNMIYSGQVISLT YTVQSGDNLSSIARRLGTTVQSLVSMN SEQ ID NO: 25 8.79 GISNPNLIYAGQTLNY Enterococcus * autolysin YTVKSGDTLNKIAAQYGVSVANLRSWN SEQ ID NO: 26 9.74 faecalis GISGD LIFVGQKLIVK YTVKSGDTLNKIAAQYGVTVANLRSWN SEQ ID NO: 27 9.74 GISGD LIFVGQKLIVK YTIKSGDTLNKIAAQYGVSVANLRSWN SEQ ID NO: 28 9.74 GISGD LIFAGQKIIVK YTIKSGDTLNKISAQFGVSVANLRSWN SEQ ID NO: 29 9.85 GIKGD LIFAGQTIIVK HTVKSGDSLWGLSMQYGISIQKIKQLN SEQ ID NO: 30 9.35 GLSGD TIYIGQTLKVG hirae * mur2 YTVKSGDSVWGISHSFGITMAQLIEWN SEQ ID NO: 31 9.35 NIKNN FIYPGQKLTIK YTVKSGDSVWKIANDHGISMNQLIEWN SEQ ID NO: 32 7.14 NIKNN FVYPGQQLVVS YTVKAGESVWSVSNKFGISMNQLIQWN SEQ ID NO: 33 9.91 NIKNN FIYPGQKLIVK YTVKAGESVWGVANKNGISMNQLIEWN SEQ ID NO: 34 9.64 NIKNN FIYPGQKLIVK YTVKAGESVWGVANKHHITMDQLIEWN SEQ ID NO: 35 7.31 NIKNN FIYPGQEVIVK YTVKAGESVWGVADSHGITMNQLIEWN SEQ ID NO: 36 7.15 NIKNN FIYPGQQLIVK Listeria * P60 VVVEAGDTLWGIAQSKGTTVDAIKKAN SEQ ID NO: 37 8.61 monocytogenes NLTTD KIVPGQKLQVN NAVKSGDTIWALSVKYGVSVQDIMSWN SEQ ID NO: 38 9.35 NLSSS SIYVGQKLAIK innocua * P60 VVVEAGDTLWGIAQSKGTTVDAIKKAN SEQ ID NO: 39 8.61 NLTTD KIVPGQKLQVN HNVKSGDTIWALSVKYGVSVQDIMSWN SEQ ID NO: 40 8.35 NLSSS SIYVGQKPAIK ivanovii * P60 VVVEAGDTLWGIAQDKGTTVDALKKAN SEQ ID NO: 41 6.35 NLTSD KIVPGQKLQIT YTVKSGDTIWALSSKYGTSVQNIMSWN SEQ ID NO: 42 9.37 NLSSS SIYVGQVLAVK YTVKSGDTLSKIATTFGTTVSKIKALN SEQ ID NO: 43 9.89 GLNSD NLQVGQVLKVK seeligeri * P60 VVVEAGDTLWGIAQDNGTTVDALKKAN SEQ ID NO: 44 6.35 KLTTD KIVPGQKLQVT HTVKSGDTIWALSVKYGASVQDLMSWN SEQ ID NO: 45 8.64 NLSSS SIYVGQNIAVK YTVKSGDTLGKIASTFGTTVSKIKALN SEQ ID NO: 46 9.62 GLTSD NLQVGDVLKVK welshimeri * P60 VVVEAGDTLWGIAQSKGTTVDALKKAN SEQ ID NO: 47 8.61 NLTSD KIVPGQKLQVT HTVKSGDTIWALSVKYGASVQDLMSWN SEQ ID NO: 48 9.35 NLSSS SIYVGQKIAVK YTVKSGDSLSKIANTFGTSVSKIKALN SEQ ID NO: 49 9.89 NLTSD NLQVGTVLKVK grayi * P60 VVVASGDTLWGIASKTGTTVDQLKQLN SEQ ID NO: 50 9.42 KLDSD RIVPGQKLTIK YKVKSGDTIWALSVKYGVPVQKLIEWN SEQ ID NO: 51 9.57 NLSSS SIYVGQTIAVK YKVQNGDSLGKIASLFKVSVADLTNWN SEQ ID NO: 52 8.59 NLNATITIYAGQELSVK Haemophilus * amiB HIVKKGESLGSLSNKYHVKVSDIIKLN SEQ ID NO: 53 10.11 influenzae QLKRK TLWLNESIKIP HKVTKNQTLYAISREYNIPVNILLSLN SEQ ID NO: 54 10.49 PHLKNG KVITGQKIKLR * yebA YTVTEGDTLKDVLVLSGLDDSSVQPLI SEQ ID NO: 55 3.87 ALDPELAHLKAGQQFYWI lppB YKVNKGDTMFLIAYLAGIDVKELAALN SEQ ID NO: 56 6.40 NLSEPNYNLSLGQVLKIS somnus lppB YKVRKGDTMFLIAYISGMDIKELATLN SEQ ID NO: 57 8.56 NMSEPYHLSIGQVLKIA Helicobacter dniR HVVLPKETLSSIAKRYQVSISNIQLAN SEQ ID NO: 58 10.02 pylori DLKDS NIFIHQRLIIR Pseudomonas lppB YIVRRGDTLYSIAFRFGWDWKALAARN SEQ ID NO: 59 10.06 aeruginosa GIAPPYTIQVGQAIQFG Putida nlpD YIVKPGDTLFSIAFRYGWDYKELAARN SEQ ID NO: 60 9.77 GIPAPYTIRPGQPIRFS Sinorhizoblum nlpD IMVRQGDTVTVLARRFGVPEKEILKAN SEQ ID NO: 61 10.27 meliloti GLKSASQVEPGQRLVIP Synechocystis nlpD HQVKEGESLWQISQAFQVDAKAIALAN SEQ ID NO: 62 4.38 sp. SISTDTELQAGQVLNIP slr0878 HVVKAGETIDSIAAQYQLVPATLISVN SEQ ID NO: 63 5.41 NQLSSGQVTPGQTILIP Aquifex nlpD1 YKVKKGDSLWKIAKEYKTSIGKLLELN SEQ ID NO: 64 10.08 acolicus PKLKNRKYLRPGEKICLK YRVKRGDSLIKIAKKFGVSVKEIKRVN SEQ ID NO: 65 10.95 KLKGN RIYVGQKLKIP YRVRRGDTLIKIAKRFRTSVKEIKRIN SEQ ID NO: 66 12.11 RLKGN LIRVGQKLKIP Volvox YTIQPGDTFWAIAQRRGTTVDVIQSLN SEQ ID NO: 67 9.03 carteri PGVVPTRLQVGQVINVP f. YTIQPGDTFWAIAQRRGTTVDVIQSLN SEQ ID NO: 68 9.03 nagariensis PGVNPARLQVGQVINVP Staphylo- ProtA HVVKPGDTVNDIAKANGTTADKIAADN SEQ ID NO: 69 5.58 coccus KLADKNMIKPGQELVVD aureus lytN YTVKKGDTLSAIALKYKTTVSNIQNTN SEQ ID NO: 70 10.03 NIANPNLIFIGQKLKVP Colletotrichum cih1 HKVKSGESLTTIAEKYDTGICNIAKLN SEQ ID NO: 71 4.76 NLADPNFIDLNQDLQIP lindemuthianum YSVVSGDTLTSIAQALQITLQSLKDAN SEQ ID NO: 72 5.46 PGVVPENLNVGQKLNVP Chlamydophila aniB IVYREGDSLSKIAKKYKLSVTELKKIN SEQ ID NO: 73 9.46 KLDSD AIYAGQRLCLQ Pneumoniae CPn0593 YVVQDGDSLWLIAKRFGIPMDKIIQKN SEQ ID NO: 74 10.01 GLNHH RLFPGKVLKLP NlpD VVVKKGDFLERIARANNTTVAKLMQIN SEQ ID NO: 75 10.17 DLTTT QLKIGQVIKVP YIVQEGDSPWTIALRNHIRLDDLLKMN SEQ ID NO: 76 8.64 DLDEYKARRLKPGDQLRIR Chlamydia NlpD VIVKKGDFLERIARSNHTTVSALMQLN SEQ ID NO: 77 9.99 trachomatis DLSST QLQIGQVLRVP YVVKEGDSPWAIALSNGIRLDELLKLN SEQ ID NO: 78 10.00 GLDEQKARRLRPGDRLRIR papQ HIVKQGETLSKIASKYNIPVVELKKLN SEQ ID NO: 79 9.89 KLNSD TIFTDQRIRLP Prevotella phg HTVRSNESLYDISQQYGVRLKNIMKAN SEQ ID NO: 80 10.72 intermedia RKIVKRGIKAGDRVVL Leuconostoc lys YTVQSGDTLGAIAAKYGTTYQKLASLN SEQ ID NO: 81 9.23 oenos Ø10MC GIGSPYIIIPGEKLKVS YKVASGDTLSAIASKYGTSVSKLVSLN SEQ ID NO: 82 9.68 GLKNANYIYVGENLKIK Oenococcus Lys44 YTVRSGDTLGAIAAKYGTTYQKLASLN SEQ ID NO: 83 9.58 oeni ØfOg44 GIGSPYIIIPGEKLKVS YKVASGDTLSAIASKYGTSVSKLVSLN SEQ ID NO: 84 9.95 GLKNANYIYVGQTLRIK Thermotoga TM0409 YKVQKNDTLYSISLNFGISPSLLLDWN SEQ ID NO: 85 5.49 maritime PGLDPHSLRVGQEIVIP YTVKKGDTLDAIAKRFFTTATFIKEAN SEQ ID NO: 86 9.73 QLKSY TIYAGQKLFIP TM1686 HVVKRGETLWSIANQYGVRVGDIVLIN SEQ ID NO: 87 8.76 RLEDPDRIVAGQVLKIG Treponema dniR HTIRSGDTLYALARRYGLGVDTLKAHN SEQ ID NO: 88 10.58 pallidum RAHSATHLKIGQKLIIP HVVQQGDTLWSLAKRYGVSVENLAEEN SEQ ID NO: 89 4.81 NLAVDATLSLGMILKTP TP0155 YEVREGDVVGRIAQRYDISQDAIISLN SEQ ID NO: 90 9.58 KLRSTRALQVGQLLKIP TP0444 HVIAKGETLFSLSRRYGVPLSALAQAN SEQ ID NO: 91 10.98 NLANVHQLVPGQRIVVP Borrelia BB0262 HKIKPGETLSHVAARYQITSETLISFN SEQ ID NO: 92 9.72 burgdorferi EIKDVRNIKPNSVIKVP YIVKKNDSISSIASAYNVPKVDILDSN SEQ ID NO: 93 4.58 NLDNE VLFLGQKLFIP * B80625 YKVVKGDTLFSIAIKYKVKVSDLKRIN SEQ ID NO: 94 10.02 KLNVD NIKAGQILIIP YTAKEGDTIESISKLVGLSQEEIIAWN SEQ ID NO: 95 5.00 DLRSK DLKVGMKLVLT YMVRKGDSLSKLSQDFDISSKDILKFN SEQ ID NO: 96 9.20 FLNDD KLKIGQQLFLK HYVKRGETLGRIAYIYGVTAKDLVALN SEQ ID NO: 97 10.05 GNRAI NLKAGSLLNVL HSVAVGETLYSIARHYGVLIEDLKNWN SEQ ID NO: 98 7.41 NLSSN NIMHDQKLKIF BB0761 YKVKKGDTFFKIANKINGWQSGIATIN SEQ ID NO: 99 9.34 LLDSP AVSVGQEILIP Lactobacillus * lys YTVVSGDSWNKIAQRNGLSMYTLASQN SEQ ID NO: 100 9.83 Øgle GKSIYSTIYPGNKLIIK Bacillus * lytE IKVKKGDTLWDLSRKYDTTISKIKSEN SEQ ID NO: 101 9.55 subtilis HLRSD IIYVGQTLSIN YKVKSGDSLWKISKKYGMTINELKKLN SEQ ID NO: 102 10.16 GLKSD LLRVGQVLKLK YKVKSGDSLSKIASKYGTTVSKLKSLN SEQ ID NO: 103 10.03 GLKSD VIYVNQVLKVK spoV1D CIVQQEDTIERLCERYEITSQQLIRMN SEQ ID NO: 104 4.20 SLALDDELKAGQILYIP yaaH MVKQGDTLSAIASQYRTTTNDITETN SEQ ID NO: 105 3.89 EIPNPDSLVVGQTIVIP YDVKRGDTLTSIARQFNTTAAELARVN SEQ ID NO: 106 10.32 RIQLNTVLQIGFRLYIP yhdD IKVKSGDSLWKLAQTYNTSVAALTSAN SEQ ID NO: 107 9.56 HLSTT VLSIGQTLTIP YTVKSGDSLWLIANEFKNTVQELKKLN SEQ ID NO: 108 9.62 GLSSD LIRAGQKLKVS YKVQLGDSLWKIANKVNMSIAELKVLN SEQ ID NO: 109 9.72 NLKSD TIYVNQVLKTK YTVKSGDSLWKIANNYNLTVQQIRNIN SEQ ID NO: 110 9.65 NLKSD VLYVGQVLKLT YTVKSGDSLWVIAQKFNVTAQQIREKN SEQ ID NO: 111 9.72 NLKTD VLGVGQKLVIS yojL IKVKSGDSLWKLSRQYDTTISALKSEN SEQ ID NO: 112 9.93 KLKST VLYVGQSLKVP YTVAYGDSLWMIAKNHKMSVSELKSLN SEQ ID NO: 113 9.81 SLSSD LIRPGQKLKIK YTVKLGDSLWKIANSLNMTVAELKTLN SEQ ID NO: 114 9.27 GLTSD TLYPKQVLKIG YKVKAGDSLWKIANRLGVTVQSIRDKN SEQ ID NO: 115 9.84 NLSSD VLQIGQVLTIS yocH ITVQKGDTLWGISQKNGVNLKDLKEWN SEQ ID NO: 116 9.25 KLTSD KIIAGEKLTIS YTIKAGDTLSKIAQKFGTTVNNLKVWN SEQ ID NO: 117 9.64 NLSSD MIYAGSTLSVK ykvP HHVTPGETLSIIASKYNVSLQQLMELN SEQ ID NO: 118 8.65 HFKSD QIYAGQIIKIR * xlyB YHVKKGDTLSGIAASHGASVKTLQSIN SEQ ID NO: 119 9.72 HITDPNHIKIGQVIKLP yrbA NIVQKGDSLWKIAEKYGVDVEEVKKLN SEQ ID NO: 120 8.51 TQLSNPDLIMPGMKIKVP ydhD HIVGPGDSLFSIGRRYGASVDQIRGVN SEQ ID NO: 121 5.49 GLDET NIVPGQALLIP ykuD YQVKQGDTLNSIAADFRISTAALLQAN SEQ ID NO: 122 6.10 PSLQA GLTAGQSIVIP ØPBSX * xlyA YVVKQGDTLTSIARAFGVTVAQLQEWN SEQ ID NO: 123 4.65 NIEDPNLIRVGQVLIVS Ø PZA * orf15 YKVKSGDNLTKIAKKHNTTVATLLKLN SEQ ID NO: 124 10.23 PSIKDPNMIRVGQTINVT (= Ø-29) HKVKSGDTLSKIAVDNKTTVSRLMSLN SEQ ID NO: 125 10.17 PEITNPNHIKVGQTIRLS Ø B103 * orf15 HVVKKGDTLSEIAKKIKTSTKTLLELN SEQ ID NO: 126 10.11 PTIKNPNKIYVGQRINVG YKIKRGETLTGIAKKNKTTVSQLMKLN SEQ ID NO: 127 10.61 PNIKNANNIYAGQTIRLK sphaericus * Pep I ILIRPGDSLWYFSDLFKIPLQLLLDSN SEQ ID NO: 128 8.86 RNINPQ LLQVGQRIQIP YTITQGDSLWQIAQNKNLPLNAILLVN SEQ ID NO: 129 7.15 PEIQPS RLHIGQTIQVP Salmonella nlpD YTVKKGDTLFYIAWITGNDFRDLAQRN SEQ ID NO: 130 8.64 dublin SISAPYSLNVGQTLQVG Escherichia * yebA YVVSTGDTLSSILNQYGIDMGDISQLA SEQ ID NO: 131 4.13 coli AADKELRNLKIGQQLSWT mltD YTVRSGDTLSSIASRLGVSTKDLQQWN SEQ ID NO: 132 10.58 KLRGS KLKPGQSLTIG YRVRKGDSLSSIAKRHGVNIKDVMRWN SEQ ID NO: 133 10.18 SDTAN LQPGDKLTLF UUG YTVKRGDTLYRISRTTGTSVKELARLN SEQ ID NO: 134 10.16 GISPPYTIEVGQKLKLG nlpD YTVKKGDTLFYIAWITGNDFRDLAQRN SEQ ID NO: 135 8.64 NIQAPYALNVGQTLQVG Drosophila Q9VNAI YTVGNRDTLTSVAARFDTTPSELTHLN SEQ ID NO: 136 7.15 melanogaster RLNSS FIYPGQQLLVP Drosophila Q961P8 YTVGNRDTLTSVAARFDTTPSELTHLN SEQ ID NO: 136 7.15 melanogaster RLNSS FIYPGQQLLVP Caenorhabditis F43G9.2 RKVKNGDTLNKLAIKYQVNVAEIKRVN SEQ ID NO: 137 10.01 elegans NMVSEQDFMALSKVKIP Caenorhabditis F52E1.13 YTITETDTLERVAASNDCTVGELMKLN SEQ ID NO: 138 7.08 elegans KMASR MVFPGQKILVP Caenorhabditis F07G11.9 TEIKSGDSCWNIASNAKISVERLQQLN SEQ ID NO: 139 8.32 elegans KGMKCDKLPLGDKLCLA LKLKAEDTCFKIWSSQKLSERQFLGMN SEQ ID NO: 140 7.84 EGMDCDKLKVGKEVCVA HKIQKGDTCFKIWTTNKISEKQFRNLN SEQ ID NO: 141 8.65 KGLDCDKLEIGKEVCIS LKIKEGDTCYNIWTSQKISEQEFMELN SEQ ID NO: 142 4.54 KGLDCDKLEIGKEVCVT YRFKKGDTCYKIWTSHKMSEKQFRALN SEQ ID NO: 143 9.35 RGIDCDRLVPGKELCVG ITVKPGDTCFSIWTSQKMTQQQFMDIN SEQ ID NO: 144 4.21 PELDCDKLEIGKEVCVT VKINPGDTCFNIWTSQRMTQQQFMDLN SEQ ID NO: 145 6.30 KRLDCDKLEVGKEVCVA VQINPGDTCFKIWSAQKLTEQQFMELN SEQ ID NO: 146 4.60 KGLDCDRLEVGKEVCIA TEVKEGDTCFKIWSAHKITEQQFMEMN SEQ ID NO: 147 5.12 RGLDCNRLEVGKEVCIV IKVKEGDTCFKIWSAQKMTEQQFMEMN SEQ ID NO: 148 7.85 RGLDCNKLMVGKEVCVS ATITPGNTCFNISVAYGINLT   DLQ SEQ ID NO: 149 3.99 KTYDCKALEVGDTICVS IEVIKGDTCWFLENAFKTNQTEMERAN SEQ ID NO: 150 4.67 EGVKCDNLPIGRMMCVW Caenorhabditis T01C4.1 HTIKSGDTCWKIASEASISVQELEGLN SEQ ID NO: 151 5.01 elegans SKKSCANLAVGLSEQEF IHVKEGDTCYTIWTSQHLTEKQFMDMN SEQ ID NO: 152 4.12 EELNCGMLEIGNEVCVD ATVTPGSSCYTISASYGLNLAELQTTY SEQ ID NO: 153 3.07 NCDALQVDDTICVS IEILNGDTCGFLENAFQTNNTEMEIAN SEQ ID NO: 154 3.85 EGVKCDNLPIGRMMCVW Bacillus # ypbE HTVQKKETLYRISMKYYKSRTGEEKIR SEQ ID NO: 155 9.45 subtilis AYNHLNGNDVYTGQVLDIP Citrobacter # eae YTLKTGESVAQLSKSQGISVPVIWSLN SEQ ID NO: 156 8.59 fruendii KHLYSSESEMMKASPGQQIILP Escherichia # eae YTLKTGETVADLSKSQDINLSTIWSLN SEQ ID NO: 157 5.65 coli KNLYSSESEMMKAAPGQQIILP Micrococcus # rpf IVVKSGDSLWTLANEYEVEGGWTALYE SEQ ID NO: 158 3.85 luteus ANKGAVSDAAVIYVGQELVL Bacillus # yneA IEVQQGDTLWSIADQVADTKKINKNDF SEQ ID NO: 159 3.81 subtilis IEWVADKNQLQTSDIQPGDELVIP Streptococcus # YTVKYGDTLSTIAEAMGIDVHVLGDIN SEQ ID NO: 160 4.23 pyogenes HIANIDLIFPDTILTANYNQHGQATTL T Bacillus # xkdP YTVKKGDTLWDIAGRFYGNETQWRKIW SEQ ID NO: 161 11.23 subtilis NANKTAMIKRSKRNIRQPGHWIFPGQK LKIP Bacillus # yqbP YTVKKGDTLWDIAGRFYGNSTQWRKIW SEQ ID NO: 161 11.23 subtilis NANKTAMIKRSKRNIRQPGHWIFPGQK LKIP Bacillus # YTVKKGDTLWDLAGKFYGDSTKWRKIW SEQ ID NO: 162 10.75 subtilis KVNKKAMIKRSKRNIRQPGHWIFPGQK LKIP Lactococcus 245-287 (33) 437 U1769600 muramidase lactis 321-363 (31) 395-437 194-237 QGCI25 258-303 319-361 ØTuc2009 332-375 (10) 428 L31364 glycosidase (muramidase) 386-428 Ø-LC3 333-376 (10) 429 U04309 muramidase 387-429 Enterococcus 363-405 (25) 671 P37710 muramidase faecalis 431-473 (25) 499-541 (25) 567-609 (19) 629-671 hirae 257-299 (38) 666 P39046 muramidase 338-380 (33) 414-456 (32) 489-531 (33) 565-607 (15) 623-665 Listeria  30-72  (130) 484 P21171 adherence and monocytogenes invasion protein P60 203-245 innocua  30-72  (129) 481 Q01836 adherence and invasion protein P60 201-243 ivanovii  30-72  (125) 524 Q01837 adherence and invasion protein P60 198-240 (73) 314-356 seeligeri  30-72  (127) 523 Q01838 adherence and invasion protein P60 200-242 (77) 320-362 welshimeri  30-72  (125) 524 M80348 adherence and invasion protein P60 198-240 (75) 316-358 grayi  30-72  (104) 511 Q01835 adherence and invasion protein P60 177-219 (79) 299-342 Haemophilus 294-336 432 P44493 N—acetylmuramoyl- influenzae L-alanine amidase 387-430 131-174 475 P44693 homologous to endopeptidase of Staphylococcus 147-190 405 P44833 outer membrane lipoprotein somnus 120-164 279 L10653 outer membrane lipoprotein Helicobacter 319-361 372 AE000654 regulatory protein pylori DniR Pseudomonas  69-113 297 P45682 Lipoprotein aeruginosa Putida  44-87 244 Y19122 lipoprotein Sinorhizoblum 166-209 512 U81296 Lipoprotein meliloti Synechocystis  87-130 715 D90915 Lipoprotein sp.   4-47 245 D90907 Hypothetical protein Aquifex  26-70  (24) 349 AE000700 Lipoprotein acolicus  95-137 (37) 174-216 Volvox  42-85 309 AF058716 chitinase carteri f. 106-149 nagariensis Staphylo- 431-474 524 A04512 protein A coccus 177-220 383 AF106851 autolysin homolog aureus Colletotrichum 110-153 (31) 230 AJ001441 glycoprotein lindemuthianum 185-228 Chlamydophila 159-201 205 AE001659.1 N—Acetylmuramoyl- L-Ala Amidase Pneumoniae 316-358 362 AE001643 124-166 233 AE001670 Muramidase 188-233 Chlamydia 138-180 245 AE001348 Muramidase trachomatis 200-245 155-197 200 AE001330 Prevotella 266-309 309 AF017417 hemagglutinin intermedia Leuconostoc 335-378 432 endolysin oenos Ø10MC 389-432 Oenococcus 335-378 432 AF047001 Lysin oeni ØfOg44 389-432 Thermotoga  26-69 271 AE001720 maritime  76-118 212-255 395 AE001809 Treponema 607-650 779 AE001237 membrane-bound pallidum lytic murein transglycosylase D 734-777  87-130 371 AE001200  67-110 342 AE001221 Borrelia 183-226 (6) 417 AE001137 Hypothetical protein burgdorferi 233-275  44-86  (28) 697 AE001164 N—acetylmuramoyl- L-alanine amidase 115-157 (7) 165-207 (8) 216-258 (27) 286-328  59-102 295 AE001176 Lactobacillus 399-442 442 X90511 lysin Øgle Bacillus  28-70  (17) 334 U38819.1 D-Glutamate-M- subtilis diam inopimlate endopeptidase  88-130 (20) 151-193 525-568 575 P37963 stage VI sporulation protein D   1-43  (5) 427 P37531 Hypothetical protein  49-92  29-71  (22) 488 Y14079 Hypothetical protein  94-136 (39) 176-218 (23) 242-284 (24) 309-351  29-71  (18) 414 Z99114 similar to cell wall binding protein  90-132 (26) 159-201 (25) 227-269  28-70  (9) 287 AF027868 similar to papQ  80-122 345-387 399 Z99111 Hypothetical protein 179-222 317 Z99110 N—acetylmuramoyl- L-alanine amidase   4-48 387 Z99118 similar to spore coat protein   4-46 439 Z99107   4-46 164 Z99111 ØPBSX 161-204 297 P39800 N—acetylmuramoyl- L-alanine amidase Ø PZA 163-207 (6) 258 P11187 (=Ø-29) 214-258 P07540 Ø B103 165-209 (9) 263 X99260 lysozyme 219-263 sphaericus   3-46  (6) 396 X69507 carboxypeptidase 1  53-96 Salmonella 121-164 377 AJ006131 dublin Escherichia  77-121 419 p24204 homologous to coli endopeptidase of Staphylococcus 343-385 (16) 452 P23931 membrane-bound lytic murein transglycosylase d precursor 402-443  50-93 259 U28375 Hypothetical protein 123-166 379 P33648 Lipoprotein Drosophila 329-371 1325 AF125384 Lethal 82FD protein melanogaster Drosophila 104-146 678 AAK92873 melanogaster Caenorhabditis  12-55 179 Z79755 elegans Caenorhabditis  24-66 819 U41109 elegans Caenorhabditis  23-66  (11) 1614 U64836/ Putative elegans AF016419 Endochitinase  78-121 (21) 143-186 (21) 208-251 (19) 271-314 (20) 335-378 (23) 402-445 (21) 467-510 (37) 548-591 (44) 636-679 (66) 746-786 (8) 795-838 Caenorhabditis  23-66  (51) 1484 U70858 Putative elegans Endochitinase 118-161 (25) 187-226 (9) 236-279 Bacillus 191-136 240 L47648 subtilis Citrobacter  65-113 936 Q07591 fruendii Escherichia  65-113 934 P43261 Necessary for close coli (intimate) attachment of bacteria Micrococcus 171-218 220 Z96935 Bacterial Cytokine luteus Bacillus  40-90 105 Z73234 subtilis Streptococcus 147-103 393 U09352 pyogenes Bacillus 176-234 235 P54335 subtilis Bacillus 177-234 235 G1225954 subtilis Bacillus 161-218 219 P45932 subtilis Consensus YxVKxGDTLxxIAxxxxxxxxxLxxxNxxLxxxxxIxxGQxIxVx (SEQ ID NO: 163) repeat H IR  ESV  LS         I      I     L     L I   L     I  V                       V     V L a) Proteins listed were obtained by a homology search in the SWISSPROT, PIR, and Genbank databases with the repeats of AcmA using the BLAST program. b) *; genes encoding cell wall hydrolases. #; proteins containing repeats that are longer than the consensus sequence. c) The number of aa residues between the repeats is given between brackets. d) Number of aa of the primary translation product. e) Genbank accession number.

TABLE 4 Calculated pIs of individual repeat sequences of the AcmA and AcmD protein anchors. AcmA anchor domain AcmD anchor domain Repeat Calculated pI Repeat Calculated pI A1 9.75 D1 4.15 A2 9.81 D2 3.78 A3 10.02 D3 4.15 A1A2A3 10.03 D1D2D3 3.85

TABLE 5 Hybrid protein anchors composed of different AcmA and AcmD repeat sequences and their calculated pIs. Composition of hybrids AcmA-repeat sequence AcmD-repeat sequence Calculated pI A1A2A3 — 10.03 A1A2 D1 9.53 A1A2A3 D1D2D3 8.66 A1 D2 8.45 A3 D1D2 7.39 A1A2 D1D2D3 6.08 A3 D1D2D3 5.07 A1 D1D2D3 4.37 — D1D2D3 3.85

REFERENCES

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1. A method for obtaining cell-wall material consisting essentially of spherical peptidoglycan microparticles, said method comprising: treating a cell-wall of a Gram-positive bacterium with an acid solution, thus removing a cell-wall component selected from the group consisting of a protein, a lipoteichoic acid, a carbohydrate, and combinations thereof from said cell-wall; and recovering cell-wall material consisting essentially of spherical peptidoglycan microparticles, wherein the cell-wall material has improved capacity for binding with a proteinaceous substance comprising an N-acetyl muramidase cell-wall binding domain, homolog, or functional derivative thereof when compared to a cell-wall that has not been treated with the acid solution.
 2. The method according to claim 1, wherein said proteinaceous substance further comprises a reactive group selected from the group consisting of an antigenic determinant, an enzyme, an antibody, an antibiotic, a hormone, an aromatic substance, an inorganic particle, and a reporter molecule.
 3. The method according to claim 1, wherein said acid solution comprises an acid selected from the group consisting of acetic acid (HAc), hydrochloric acid (HCl), sulphuric acid (H₂SO₄), trichloro acetic acid (TCA), trifltuoro acetic acid (TFA), monochloric acid (MCA), and mixtures thereof.
 4. The method according to claim 3, wherein said solution comprises 0.06 to 1.2 M TCA.
 5. The method according to claim 4, wherein said solution comprises 0.6 M TCA.
 6. The method according to claim 1, wherein treating a cell-wall of a Gram-positive bacterium with an acid solution comprises heating the cell-wall in the acid solution.
 7. The method according to claim 6, comprising boiling the cell-wall in the acid solution.
 8. The method according to claim 1, wherein recovering cell-wall material comprises pelleting the cell-wall material.
 9. The method according to claim 1, wherein recovering cell-wall material comprises removing the acid solution from the cell-wall material by washing with a neutralizing solution.
 10. The method of claim 1, further comprising freezing the cell-wall material.
 11. The method of claim 1, further comprising drying the cell-wall material.
 12. The method according to claim 1, wherein said Gram-positive bacterium is selected from the group consisting of a Lactococcus, a Lactobacillus, a Bacillus and a Mycobacterium spp.
 13. The method according to claim 9 wherein the neutralizing solution is phosphate buffer saline.
 14. The method according to claim 11, wherein drying the cell-wall material comprises drying the cell-wall material under a vacuum.
 15. A method for obtaining cell-wall material consisting essentially of spherical peptidoglycan microparticles able to bind with a proteinaceous substance comprising an N-acetyl muramidase cell-wall binding domain, the method comprising: treating a cell-wall of a Gram-positive bacterium with an acid solution thus removing a component therefrom, said component selected from the group consisting of a protein, a lipoteichoic acid, a carbohydrate, and a combination of any thereof from the cell-wall, so as to obtain cell-wall material consisting essentially of spherical peptidoglycan microparticles able to bind with a proteinaceous substance comprising an N-acetyl muramidase cell-wall binding domain. 